Category: 1450754-41-2

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 1450754-41-2, name is 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol. A new synthetic method of this compound is introduced below., category: alcohols-buliding-blocks

To a solution of ethan1-ol (200 mg,145 mrnoi, 1 equiv) in tetrahydrofuran (10 mL) at 24 C, was added carbonyidiimidazole(950 mg, 580 mmol, 4.00 equiv). The mixture was allowed to stir for 12 hours at 24 eQ Theproduct mixture was concentrated in vacuo to a solid residue. The residue was directly loadedto a hexaneequilibrated silica gel column and the desired material was eluted using a 50–100% ethyl acetate-hexane solvent, two steps). The irnidazole 5 was isolated as colorless oilafter concentration of the residual soR nt (320 mRf= 0.15 (40 ethyl acetate—he?ane; LV). f- NMR (500 MHz, ()Cl.). 8.13 (s, I]1 7.42-7..-1 I ,m, IH, H-. 7.03—7.u2 ,ni. I H 4.26—4 23 a. 2Ff, 7 1 :-iz, F).L99–i.96(m.3RHR:). I H–I S8(t,2H.i==Hz.H). I 6(– I 6{t,2H.i==7.I Hz.H). ?( >R (125 MHz. CDCI ). d I?4X.3 (C). I 7. I (CH. 130 7 Ci). 117. 1 ( H), 82 3(( , 6 (( H). o2 ) {OCH). 32 QH , 32.1) (( RI, 26.0 (CN , I . I ((?Ri) IR (AE R-FTIR) cm? 3291 (brj, 3 1 8 (w) 3 132 (rn,j, 2960 (w), 2921 (m,j, 2858 (m) 1 758 (s), 1588(s). 1525 mL 1473 (m). 1444 (m), 1404 (in), 1350 (w), 1316 (w). 1282 (? . 1240 (w), 1173(w), 1095 (m), 1058 (m) 1003 (v, 898 (m), 833 , 768 (w), 749 ( 6-l (v, 598 (w),526 (w). HRMSESI (m/z) [. L calculated for C H 1N4O2, 233. 1039. Ibund. 233.1064.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 1450754-41-2, 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol.

Reference:
Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; WOO, Christina, M.; GAO, Jinxu; (555 pag.)WO2018/226828; (2018); A2;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 1450754-41-2, name is 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol. A new synthetic method of this compound is introduced below., Computed Properties of C7H10N2O

To a solution of ethan1-ol (200 mg,145 mrnoi, 1 equiv) in tetrahydrofuran (10 mL) at 24 C, was added carbonyidiimidazole(950 mg, 580 mmol, 4.00 equiv). The mixture was allowed to stir for 12 hours at 24 eQ Theproduct mixture was concentrated in vacuo to a solid residue. The residue was directly loadedto a hexaneequilibrated silica gel column and the desired material was eluted using a 50–100% ethyl acetate-hexane solvent, two steps). The irnidazole 5 was isolated as colorless oilafter concentration of the residual soR nt (320 mRf= 0.15 (40 ethyl acetate—he?ane; LV). f- NMR (500 MHz, ()Cl.). 8.13 (s, I]1 7.42-7..-1 I ,m, IH, H-. 7.03—7.u2 ,ni. I H 4.26—4 23 a. 2Ff, 7 1 :-iz, F).L99–i.96(m.3RHR:). I H–I S8(t,2H.i==Hz.H). I 6(– I 6{t,2H.i==7.I Hz.H). ?( >R (125 MHz. CDCI ). d I?4X.3 (C). I 7. I (CH. 130 7 Ci). 117. 1 ( H), 82 3(( , 6 (( H). o2 ) {OCH). 32 QH , 32.1) (( RI, 26.0 (CN , I . I ((?Ri) IR (AE R-FTIR) cm? 3291 (brj, 3 1 8 (w) 3 132 (rn,j, 2960 (w), 2921 (m,j, 2858 (m) 1 758 (s), 1588(s). 1525 mL 1473 (m). 1444 (m), 1404 (in), 1350 (w), 1316 (w). 1282 (? . 1240 (w), 1173(w), 1095 (m), 1058 (m) 1003 (v, 898 (m), 833 , 768 (w), 749 ( 6-l (v, 598 (w),526 (w). HRMSESI (m/z) [. L calculated for C H 1N4O2, 233. 1039. Ibund. 233.1064.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 1450754-41-2, 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol.

Reference:
Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; WOO, Christina, M.; GAO, Jinxu; (555 pag.)WO2018/226828; (2018); A2;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Electric Literature of 1450754-41-2, Adding some certain compound to certain chemical reactions, such as: 1450754-41-2, name is 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol,molecular formula is C7H10N2O, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 1450754-41-2.

(f) Imidazole (740 mg, 10.87 mmol, 3.0 eq), triphenylphosphine (1.05 g, 3.99 mmol, 1.1 eq) and dichloromethane (5 ml) were added to the reaction flask and cooled to 0 C.Add iodine (1.1 g, 4.35 mmol, 1.2 eq), and add the incubation reaction for 30 minutes.A solution of compound 5 (500 mg, 3.62 mmol, 1 eq) in dichloromethane (1 ml) was added at low temperature, and the mixture was stirred for 4 hours.Quenched with saturated sodium sulfite solution, extracted with ethyl acetate, dried and dried.Purified by column to obtain 400 mg of compound 6, yield: 46%

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 1450754-41-2, 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Suzhouguangdian Biological Technology Co., Ltd.; Ni Runyan; Wang Wei; (8 pag.)CN109369532; (2019); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Electric Literature of 1450754-41-2, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 1450754-41-2, name is 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol, molecular formula is C7H10N2O, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

4-[4-[[[[4-Chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]phenoxy]-2-picolinic acid (0.065) with a monocarboxylic acid g, 0.145mmol)Dissolved in 3mL anhydrous tetrahydrofuran solution,Add EDC·HCl (0.04 g, 0.218 mmol),HOBT (0.024g, 0.174mmol)Stir well at 0 C,Then DIPEA (0.094 g, 0.725 mmol) was added dropwise and stirred for 1 h.A linker (0.02 g, 0.145 mmol) containing a photoaffinity group diaziridine and an alkynyl group was added.Stir at room temperature for 24 h, after the reaction is over,The organic solvent was removed by a low pressure, and the mixture was washed with water and saturated aqueous sodium hydrogen carbonate. The organic phase obtained after washing with saturated brine was dried over anhydrous sodium sulfate and evaporated. Separating the crude product by column separation,The title compound was obtained by eluting with petroleum ether / ethyl acetate (V/V = 1/3), weight: 0.12 g, yield 14.7%.A compound represented by the general formula (X) based on the VEGFR-2 inhibitor sorafenib photoaffinity probe was obtained.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 1450754-41-2, 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol.

Reference:
Patent; Xi’an Jiaotong University; Zhang Jie; Lu Wen; Wang Sicen; Pan Xiaoyan; He Langchong; Sun Ying; Wang Jin; Song Jie; (9 pag.)CN109456261; (2019); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 1450754-41-2, name is 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol, molecular formula is C7H10N2O, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. Safety of 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol

(f) imidazole (740 mg, 10.87 mmol, 3.0 eq),Triphenylphosphine (1.05 g, 3.99 mmol, 1.1 eq)Add dichloromethane (5ml) to the reaction flask and cool to 0 C.Add iodine (1.1 g, 4.35 mmol, 1.2 eq),Add the insulation reaction for 30 minutes.Add compound 5 (500 mg, 3.62 mmol, 1 eq) at low temperatureA solution of methylene chloride (1 ml) was added and the reaction was kept for 4 hours.Quenched with saturated sodium sulfite solution, extracted with ethyl acetate.Dry, spin dry, and purified by column to obtain 400 mg of compound 6,Yield: 46%

With the rapid development of chemical substances, we look forward to future research findings about 1450754-41-2.

Reference:
Patent; Suzhouguangdian Biological Technology Co., Ltd.; Ni Runyan; Wang Wei; (7 pag.)CN109438211; (2019); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Reference of 1450754-41-2 ,Some common heterocyclic compound, 1450754-41-2, molecular formula is C7H10N2O, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido)phenyl)picolinic acid, an intermediate with a monocarboxylic acid(0.063g, 0.145mmol)Dissolved in 3mL anhydrous tetrahydrofuran solution,Add EDC¡¤HCl (0.04 g, 0.218 mmol),HOBT (0.024 g, 0.174 mmol) was stirred well at 0 C, then DIPEA (0.094 g, .725 mmol) was added dropwise and stirred.1h,Add inPhotoaffinity group dipyridiniumAlkynyl chainConnector(0.02g, 0.145mmol),Stir at room temperature for 24 h,After the reaction is completed, the solvent is removed under reduced pressure, and an appropriate amount of ethyl acetate is added thereto, followed by washing with water and washing with saturated sodium hydrogen carbonate, and then sat.Washed with brine, combined with EtOAc (EtOAc m.The target compound was obtained, and weighed 0.03 g, yield 41.66%. Obtaining a general formula based on the VEGFR-2 inhibitor B14 photoaffinity probe

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 1450754-41-2, 2-(3-But-3-ynyl-3H-diazirin-3-yl)-ethanol, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Xi’an Jiaotong University; Zhang Jie; Lu Wen; Wang Sicen; Pan Xiaoyan; He Langchong; Sun Ying; Wang Jin; Song Jie; (10 pag.)CN109503553; (2019); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts