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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893465Generated: October 31, 2026

Benzylamine → HCID 25120534, compound

https://huagongshe.com/reaction/1893465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 25120537HCID 25120537—
SolventMethanolHCID 887—
ProductHCID 25120534HCID 25120534—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a solution of the benzylamine (13 μL, 0.12 mmol) in methanol (400 μL) was added 4-[(3-hydroxypropyl)amino]-7-(trifluoromethyl)imidazo[1,2-a]quinoxaline-1-carbaldehyde (35 mg, 0.10 mmol). The reaction mixture was stirred at 30° C. for 17 h. After addition of NaBH4 (5 mg, 0.12 mmol), the mixture was stirred at 30° C. for 5 h. Then it was concentrated, diluted in ethyl acetate, washed with an aqueous saturated solution of ammonium chloride and extracted with ethyl acetate. The combined organic phases were dried over Na2SO4, filtered, concentrated in vacuo to give, after purification by preparative TLC (dichloromethane/methanol 9/1), the title compound (32 mg, 75%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-ac4bf4e628644a6488e8995bfd93ae62
Source noteuspto-grants-2013_08