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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893463Generated: October 31, 2026

Sodium borohydride → HCID 59333317, compound

https://huagongshe.com/reaction/1893463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 25120537HCID 25120537—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 59333317HCID 5933331761%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the 4-[(3-hydroxypropyl)amino]-7-(trifluoromethyl)imidazo[1,2-a]quinoxaline-1-carbaldehyde prepared as in example 36 (8 mg, 0.024 mmol) in anhydrous methanol (300 μL), cooled at 0° C. was added sodium borohydride (2 mg, 0.047 mmol). The mixture was allowed to warm to room temperature over 1 h under argon and then diluted with water and extracted three times with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and evaporated. The crude product was purified by preparative TLC (silica gel, dichloromethane/methanol 9/1) to afford the title compound as a white solid (5 mg, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-b779f65da13f4cc3b3bb7319c72d9781
Source noteuspto-grants-2013_08