Category: 84832-00-8

Adding a certain compound to certain chemical reactions, such as: 84832-00-8, (5-Amino-2-fluorophenyl)methanol, 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, 84832-00-8, blongs to alcohols-buliding-blocks compound. Quality Control of (5-Amino-2-fluorophenyl)methanol

Example 205 : 1 -(2-Fluoro-5 -morpholinobenzyl)-N-( 1 -methyl- 1 H-pyrazol-4-yl)- 1 H- pyrazo lo [3 ,4-d]pyrimidin-6-amineStep (i) To a solution of 5-Amino-2-fluoro benzyl alcohol (500mg, 3.5mmol) in toluene (12mL) was added DIEA (2eq) and 2-bromoethylether (1.5eq) and the reaction heated to 90C for 18h. The solvent was removed in vacuo and the residue partitioned between EtOAc and H20. The organic phase was dried (Na2S04), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (petroleum ether: EtOAc) to give 2(2-fluoro-5- morpholinophenyl)methanol (550mg, 74%) as a yellow oil.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,84832-00-8, its application will become more common.

Reference:
Patent; CELLZOME LIMITED; RAMSDEN, Nigel; HARRISON, Richard John; OXENFORD, Sally; BELL, Kathryn; PITON, Nelly; DAGOSTIN, Claudio; BOUSSARD, Cyrille; RATCLIFFE, Andrew; WO2011/48082; (2011); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Related Products of 84832-00-8 ,Some common heterocyclic compound, 84832-00-8, molecular formula is C7H8FNO, 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.

Intermediate 4; (2-Flu or o-5-hvdrazinylphenyl)methanol hydrochloride; (5-Amino-2-fluorophenyl)methanol (3.6 g, 25.8 mmol) was dissolved in cone. HCl (39 ml) and cooled to 00C. A solution OfNaNO2 (1.89g, 27.4 mmol) in water (9.4 ml) was added dropwise during 20 minutes at O0C. The mixture was stirred for 15 minutes and a solution of SnCl2 (1 Ig, 57.4 mmol) in cone. HCl (11.5 ml) was added dropwise. The mixture was allowed to stir for 60 minutes at O0C and basified by addition of aqueous 14N NaOH and extracted with EtOAc. The organic phase was washed with brine and extracted with a solution of HCl (1 M). The water phase was freeze-dried to give the title compound (1.65 g, 33%). APCI-MS m/z: 157 [MH+].

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,84832-00-8, its application will become more common.

Reference:
Patent; ASTRAZENECA AB; WO2009/82342; (2009); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts