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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515957Generated: October 26, 2026

Ammonium Hydroxide → HCID 53251801, compound

https://huagongshe.com/reaction/515957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantMethyl 4-(bromomethyl)-2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-6-(3-(trifluoromethyl)phenylamino)pyrimidine-5-carboxylateHCID 67238407—
SolventTetrahydrofuranHCID 8028—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 53251801HCID 532518013%

Reaction Steps

A mixture of methyl 4-(bromomethyl)-2-((1R,2S)-2-(tert-butoxycarbonyl-amino)cyclohexylamino)-6-(3-(trifluoromethyl)phenylamino)pyrimidine-5-carboxylate (120 mg, 0.199 mmol) in THF was treated with ammonium hydroxide. The reaction mixture was stirred at RT overnight, and subsequently worked up and purified by reverse phase preparative HPLC. The fractions were collected and concentrated under reduced pressure to give a residue, which was treated with TFA/DCM. The final product was purified again by preparative HPLC. Lyophilization gave a TFA salt of the title compound as a white solid (2.6 mg, 3%). [M+H] calc'd for C19H21F3N6O, 407; found, 407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108970B2
Source datasetuspto-grants-2015_08
ORD IDord-e036ac6febd24a818003389875e4b9c7
Source noteuspto-grants-2015_08