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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454760Generated: October 31, 2026

Sodium borohydride → HCID 57530960, compound

https://huagongshe.com/reaction/1454760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67350239HCID 67350239—
SolventMethanolHCID 887—
ProductHCID 57530960HCID 5753096098.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

2-Fluoro-6-[(4,6-dimethoxypyrimidin-2-yl)carbonyl]aniline 2.68 g (9.67 mmol) was dissolved in methanol 80 ml and, after cooling it to 5° C., sodium borohydride 0.73 g (19.33 mmol) was added thereto while stirring. Then the solution was stirred at room temperature for 2 hours. The reaction solution was distilled off under reduced pressure and the obtained crystals were dissolved in water and dichloromethane. The organic layer was separated and the water layer was further extracted three times with dichloromethane. After the organic layer had been washed with water and dried, dichloromethane was distilled off under reduced pressure to obtain the objective 2-fluoro-6-[(4,6-dimethoxypyrimidin-2-yl)hydroxymethyl]aniline 2.66 g (yield 98%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482308B2
Source datasetuspto-grants-2009_01
ORD IDord-d78ddbb740764b7387a180035a53e104
Source noteuspto-grants-2009_01