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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17002Generated: October 29, 2026

2-Tert-butoxycarbonylamino-3-thiazol-2-ylpropionic acid methyl ester → (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(1,3-thiazol-2-yl)propanoic acid

https://huagongshe.com/reaction/17002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Tert-butoxycarbonylamino-3-thiazol-2-ylpropionic acid methyl esterHCID 67392065—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(1,3-thiazol-2-yl)propanoic acidHCID 1118485742.8%

Reaction Steps

To 2-tert-butoxycarbonylamino-3-thiazol-2-ylpropionic acid methyl ester (500 mg, 1.75 mmol) in a mixture of acetonitrile (6 mL) and 0.2 M aqueous NaHCO3 (12 mL) was added Alcalase (2.4 L, 0.08 mL), and the solution was stirred vigorously at room temperature for about 2.5 h. The reaction mixture was then evaporated at 30° C. to remove acetonitrile, and the aqueous residue was washed with ether. The aqueous phase was acidified with 6 N HCl to pH 3 and the solution was extracted with ethyl acetate. The combined organic layers were then dried and evaporated to yield 2(S)-tert-butoxycarbonylamino-3-thiazol-2-ylpropionic acid (204 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737300B2
Source datasetuspto-grants-2010_06
ORD IDord-5278f9f0def04cecb0265400d0adbc10
Source noteuspto-grants-2010_06