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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250872Generated: October 30, 2026

(2S)-3-{4-[3-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-propoxy]-phenyl}-2-(toluene-4-sulfonylamino)-propionic acid tert-butyl ester → (2S)-3-{4-[3-(1,4,5,6-Tetrahydropyrimidin-2-ylcarbamoyl)-propoxy]-phenyl}-2-(toluene4-sulfonylamino)-propionic acid

https://huagongshe.com/reaction/1250872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-3-{4-[3-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-propoxy]-phenyl}-2-(toluene-4-sulfonylamino)-propionic acid tert-butyl esterHCID 57120024—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acid waterHCID 22392675—
Product(2S)-3-{4-[3-(1,4,5,6-Tetrahydropyrimidin-2-ylcarbamoyl)-propoxy]-phenyl}-2-(toluene4-sulfonylamino)-propionic acidHCID 9913985—

Reaction Steps

240 mg of (2S)-3-{4-[3-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-propoxy]-phenyl}-2-(toluene-4-sulfonylamino)-propionic acid tert-butyl ester were dissolved in 5 ml of methylene chloride and 1.6 ml of trifluoroacetic acid/water (95/5). The mixture was stirred for 2 hours at ambient temperature. The solvents were removed in vacuo. The residue was triturated with diethyl ether, filtered and dried in vacuo. Yield 196 mg. MS (ES+): m/e=503.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-f84b3c1c20f54bd690ced4c2fbde5efa
Source noteuspto-grants-2002_01