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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19599Generated: October 30, 2026

Trifluoroacetic acid → 4-(aminomethyl)-N-[4-[[5-[3-(4-methoxyphenyl)phenyl]pyrazolo[1,5-c]pyrimidin-7-yl]amino]phenyl]benzamide;2,2,2-trifluoroacetic acid

https://huagongshe.com/reaction/19599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(4-{4-[5-(4'-Methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidin-7-ylamino]-phenylcarbamoyl}-benzyl)-carbamic acid tert-butyl esterHCID 67319203—
SolventDichloromethaneHCID 6344—
Product4-(aminomethyl)-N-[4-[[5-[3-(4-methoxyphenyl)phenyl]pyrazolo[1,5-c]pyrimidin-7-yl]amino]phenyl]benzamide;2,2,2-trifluoroacetic acidHCID 86616044—

Reaction Steps

A mixture of (4-{4-[5-(4′-methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidin-7-ylamino]-phenylcarbamoyl}-benzyl)-carbamic acid tertbutyl ester (0.124 g) and trifluoroacetic acid (TFA)(1.5 ml) in dichloromethane (7 ml) is stirred 3 h at ambient temperature. The reaction mixture is evaporated, coevaporated with toluene and dried at high vacuum. Crystals (0.136 g) are obtained in quantitative yield and a melting temperature at 235-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745446B2
Source datasetuspto-grants-2010_06
ORD IDord-57a3d0e890dd429fba0b7666139983ab
Source noteuspto-grants-2010_06