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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454761Generated: October 31, 2026

Sodium borohydride → 2-Chloro-6-[(4,6-dimethoxypyrimidin-2-yl)methyl]aniline

https://huagongshe.com/reaction/1454761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-6-[1-(4,6-dimethoxypyrimidin-2-yl)-1-methylthiomethyl]anilineHCID 57530964—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
Product2-Chloro-6-[(4,6-dimethoxypyrimidin-2-yl)methyl]anilineHCID 5753095893.3%

Reaction Steps

To 10 ml of a methanol solution of 2-chloro-6-[1-(4,6-dimethoxypyrimidin-2-yl)-1-methylthiomethyl]aniline 0.6 g (1.84 mmol) and 0.88 g (3.68 mmol) of nickel(II) chloride hexahydrate, 0.28 g (7.37 mmol) of sodium borohydride was added at 0-10° C. and the reaction solution was stirred at room temperature for 2 hours. After the reaction solution was distilled off under reduced pressure, aqueous ammonia and dichloromethane were added and the insoluble matter was filtered off. 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 and the obtained crystals were washed with n-hexane to obtain the objective 2-chloro-6-[(4,6-dimethoxypyrimidin-2-yl)methyl]aniline 0.48 g (yield 93%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482308B2
Source datasetuspto-grants-2009_01
ORD IDord-3113ff7f272645729c7b1f7a4da8b950
Source noteuspto-grants-2009_01