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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220485Generated: October 31, 2026

Sodium borohydride → HCID 58792273, compound

https://huagongshe.com/reaction/2220485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15949563HCID 15949563—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58792273HCID 58792273—

Reaction Steps

A solution of 4-{2-amino-4-[3-(2-fluoropyridin-3-yl)phenyl]-1-methyl-5-oxo-4,5-dihydro-1H-imidazol-4-yl}-1-ethyl-1H-pyrrole-2-carbaldehyde (0.071 g; 0.25 mmol) in THF (20 mL) and methanol (5 mL) was stirred at ambient temperature as an excess of NaBH4 (0.071 g; 1.88 mmol) was added. After one hour the solvents were evaporated and the residue was taken up into dichloromethane and washed with water. The dichloromethane phase was dried over MgSO4, filtered, and evaporated. The resultant residue was crystallized from ethyl acetate and hexane to obtain the title product as a white solid, mp 170-172° C.; MS (ES) m/z 406.1; [M−H]−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417047B2
Source datasetuspto-grants-2008_08
ORD IDord-e27f36afcbcb4472afc6c8b90ab6c97d
Source noteuspto-grants-2008_08