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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276367Generated: October 29, 2026

1,1-Dichloroethane → HCID 9936394, compound

https://huagongshe.com/reaction/1276367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
Reactant2,3-DichlorobenzaldehydeHCID 35745—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22115362HCID 22115362—
SolventDiethyl EtherHCID 3283—
ProductHCID 9936394HCID 9936394—

Reaction Steps

2,3-Dichlorobenzaldehyde (115 mg, 0.66 mmol, 1.5 equiv.) was added to N-(pyrrolidin-3-(RS)-ylmethyl)-2-[5-(4-methoxyphenyl)pyrimidin-2-ylthio]acetamide in dichloroethane (3.4 mL, 0.44 mmol). Excess Na(OAc)3BH (0.2 g, 0.9 mmol, ~3 equiv.) was added and the resulting suspension was stirred vigorously overnight. The reaction mixture was diluted with ether and quenched with 1 M hydrochloric acid to afford a cloudy mixture. The organic layer was carefully removed and the aqueous phase made basic with 5 M aqueous sodium hydroxide to pH 11. After thorough extraction with ethyl acetate, the combined organic phases was washed with brine, then dried over sodium sulfate and concentrated. Chromatography on silica (0-10% methanol in ethyl acetate) afforded N-(1-(2,3-dichlorobenzyl)pyrrolidin-3-(RS)-ylmethyl)-2-[5-(4-methoxyphenyl)pyrimidin-2-ylsulfanyl]acetamide that was converted to the hydrochloride salt using 4 M hydrochloric acid solution in dioxane and ether (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166015
Source datasetuspto-grants-2000_12
ORD IDord-a34b6fd293474f2180a584977693fedf
Source noteuspto-grants-2000_12