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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860438Generated: October 30, 2026

Sodium borohydride → HCID 69309219, compound

https://huagongshe.com/reaction/860438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69308208HCID 69308208—
SolventMethanolHCID 887—
ProductHCID 69309219HCID 6930921959.1%

Reaction Steps

To a solution of ethyl 4-[7-chloro-4-(4-fluorophenyl)-2-methylpyrrolo[1,2-b]pyridazin-3-yl]-3-oxo-butanoate (160 mg) in methanol (5 ml) was added sodium borohydride (23.4 mg) at 0° C. and the mixture was stirred at the same temperature for 1 hour. The mixture was partitioned between 1N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was purified by preparative thin-layer chromatograpy eluting with a mixture of ethyl acetate and hexane (1:3) and triturated with ethyl acetate to give ethyl 4-[7-chloro-4-(4-fluorophenyl)-2-methylpyrrolo[1,2-b]pyridazin-3-yl]-3-hydroxybutanoate (95 mg) as an yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-3ec3997941af4d86a2a0f6bbd65659bd
Source noteuspto-grants-2006_12