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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161775Generated: October 29, 2026

Sodium cyanoborohydride → HCID 68648374, compound

https://huagongshe.com/reaction/1161775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 68648055HCID 68648055—
ReactantHCID 68648217HCID 68648217—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 68648374HCID 68648374—

Reaction Steps

Add Preparation 10 (5.25 g) to a suspension of imidazolocyclohexy-3-amine hydrochloride (2 gm) (Preparation 8) in methanol (30 mL). Stir the mixture at room temperature for 30 min. Add sodium cyanoborohydride (1 g) and stir the mixture for 2 h. Heat the reaction mixture at 50° C. for 2 h. Dilute the reaction mixture with ethyl acetate (50 mL) and wash the mixture with water (50 mL). Dry ethyl acetate layer over sodium sulfate and concentrate on rotary evaporator to give a crude. Purify the crude by silica flash chromatography eluting with a gradient of 0-5% methanol in DCM to give the product as a mixture of diastereomers, 3-(4-benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-3H-benzimidazole-3-yl)-pyrrolidin-2-one (4.5 gm). MS: m/z=470 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820659B2
Source datasetuspto-grants-2010_10
ORD IDord-b489c842f7d94d9fbe6a491006714aac
Source noteuspto-grants-2010_10