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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276370Generated: October 31, 2026

3,4-Dichlorobenzaldehyde → HCID 22115321, compound

https://huagongshe.com/reaction/1276370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorobenzaldehydeHCID 22710—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22115344HCID 22115344—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 22115321HCID 22115321—

Reaction Steps

A stock solution containing N-(pyrrolidin-3-(RS)-ylmethyl)-2-(5-(4-methoxyphenyl)pyrimidin-2-yloxy)acetamide (0.44 mmol) in dichloroethane (10 mL) was added to a solution of 3,4-dichlorobenzaldehyde (85 mg, 0.48 mmol, 1.1 equiv.) and diisopropylethylamine (0.35 mL, 2.0 mmol, 4.5 equiv.) in dichloroethane (5 mL). Excess Na(OAc)3BH (140 mg, 0.66 mmol, 1.5 equiv.) was added and the reaction mixture was stirred rapidly at room temperature overnight. The reaction mixture was quenched with methanol, concentrated and diluted with 1:1 methanol/dimethyl sulfoxide. The solution was then purified directly using preparative reverse phase chromatography to give, after treatment with 4 M hydrochloric acid in dioxane (1 mL) and concentration, N-[1-(3,4-dichlorobenzyl)pyrrolidin-3-(RS)-ylmethyl]-2-[5-(4-methoxyphenyl)pyrimidin-2-yloxy]-acetamide HCl salt (96 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166015
Source datasetuspto-grants-2000_12
ORD IDord-d86ca6c477b04d9c9f3588d8fa087440
Source noteuspto-grants-2000_12