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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618332Generated: November 1, 2026

Potassium Carbonate → (S)-3-(tert-butoxycarbonylamino)-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoic acid

https://huagongshe.com/reaction/1618332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-methyl 3-(tert-butoxycarbonylamino)-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoateHCID 68182808—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(S)-3-(tert-butoxycarbonylamino)-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoic acidHCID 66765701—
Product(S)-3-amino-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoic acidHCID 68183011—

Reaction Steps

A suspension of (S)-methyl 3-(tert-butoxycarbonylamino)-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoate (25 mg) and K2CO3 (25.4 mg) in acetone and water (1:1, 4 mL) was stirred at room temperature for 16 hours. The mixture was acidified to pH1. Solvents were removed under vacuum and the residue was purified by preparative HPLC to give (S)-3-(tert-butoxycarbonylamino)-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoic acid (15.6 mg) and (S)-3-amino-2-(4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzamido)propanoic acid (3.9 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765944B2
Source datasetuspto-grants-2014_07
ORD IDord-dc2fbd331f2c47388937d4561b60a1d4
Source noteuspto-grants-2014_07