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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639645Generated: October 29, 2026

Sodium borohydride → HCID 67455110, compound

https://huagongshe.com/reaction/639645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86614477HCID 86614477—
SolventDichloromethaneHCID 6344—
ProductHCID 67455110HCID 6745511053.7%

Reaction Steps

(4,6-Bis-benzylamino-5-nitro-pyridin-2-yl)-acetaldehyde (250 mg, 0.66 mmol) was stirred in 15 ml dichloromethane. Sodium borohydride (38 mg, 0.99 mmol) was added and the solution stirred at ambient temperature overnight. The reaction mixture was partitioned between DCM and water, the organics dried over magnesium sulphate and concentrated to give a crude solid which was purified by column chromatography on silica, eluting with pentane:EtOAc, 4:1 to 1:1 to afford the title compound as a yellow solid, (134 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691877B2
Source datasetuspto-grants-2010_04
ORD IDord-0fae3f8999304de1913402ca10c53260
Source noteuspto-grants-2010_04