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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412481Generated: October 26, 2026

Trifluoroacetic acid → HCID 54272787, compound

https://huagongshe.com/reaction/412481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(4-Tert-butoxycarbonylamino-phenyl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionic acid tert-butyl esterHCID 53886303—
SolventDichloromethaneHCID 6344—
ProductHCID 54272787HCID 5427278764.5%

Reaction Steps

A solution of (R) 3-(4-tert-butoxycarbonylamino-phenyl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionic acid tert-butyl ester (2 g, Reference Example 11) in dichloromethane (50 mL) was treated with trifluoroacetic acid (5 mL). After four hours [the reaction was monitored by TLC: no more starting material was visible after about 4 hours] at room temperature the reaction mixture was poured carefully onto a mixture of sodium hydrogen carbonate solution (100 mL, 5% w/v) and dichloromethane (50 mL). The organic layer was separated then dried and then evaporated to give the title compound (1.0 g) as a yellow oil which slowly crystallised on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562851B2
Source datasetuspto-grants-2003_05
ORD IDord-2847da8ee73547e7bb470155cde7cae1
Source noteuspto-grants-2003_05