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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875452Generated: October 30, 2026

Sodium borohydride → HCID 71061313, compound

https://huagongshe.com/reaction/875452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86720651HCID 86720651—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71061313HCID 7106131322%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 3,5-dichloro-4-({7-[(cyclopropylcarbonyl)amino]-1H-pyrrolo[2,3-c]pyridin-3-yl}carbonyl)benzoate (100 mg, 2.31 mmol) in 1,4-dioxane and water (3:1), sodium borohydride (27 mg, 6.944 mmol) was added portion wise over a period of about 15 minutes, followed by heating the reaction mixture at 60° C. until starting material was consumed (approximately 3 hours) The reaction mixture was cooled to room temperature and quenched by the addition of saturated aq. ammonium chloride solution and extracted with ethyl acetate. Organic layer was separated, washed with brine, dried over sodium sulfate and concentrated under vacuum. Purification by silica gel (100-200) column chromatography using dichloromethane and methanol gradient as eluent afforded N-{3-[2,6-dichloro-4-(hydroxymethyl)benzoyl]-1H-pyrrolo[2,3-c]pyridin-7-yl}cyclopropane carboxamide (20 mg, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980911B2
Source datasetuspto-grants-2015_03
ORD IDord-c25363a611a6401f80f97b456af7277e
Source noteuspto-grants-2015_03