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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488418Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 69804678, compound

https://huagongshe.com/reaction/488418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22269990HCID 22269990—
ReactantHCID 53786874HCID 53786874—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69804678HCID 69804678—

Reaction Steps

106 mg of benzotriazol-1-yl-N-tetramethyl-uronium-tetrafluoroborate and 68 mg of 1-hydroxybenzotriazole are added to a solution of 200 mg of 4-[(3-bromophenyl)amino]-6-{[(2-carboxyvinyl)carbonyl]amino}-quinazoline in 2.5 ml of dimethyl-formamide. The solution is stirred for 20 minutes at ambient temperature, then 0.5 ml of Hünig's base and 148 mg of 3-{N-[(ethoxycarbonyl)methyl]-N-methylamino}propylamine, dissolved in 0.5 ml of dimethylformamide, are added. The reaction mixture is stirred for a further two hours at ambient temperature before being poured onto 50 ml of water for working king up. The aqueous phase is extracted with ethyl acetate, the combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evaporation. The crude product is purified by chromatography on a silica gel column with methylene chloride/ethanol (20:1 to 9:1). Yield: 106 mg (39% of theory), Melting point: 278-279° C. Mass spectrum (ESI*): m/z=569, 571 [M+H]*

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972288B1
Source datasetuspto-grants-2005_12
ORD IDord-fb43b63a57ed4506899e18d4f0246883
Source noteuspto-grants-2005_12