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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193707Generated: October 31, 2026

Hydrochloric Acid → 3-Oxo-3-[(1,3-thiazol-2-yl)amino]propanoic acid

https://huagongshe.com/reaction/2193707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant2-AminothiazoleHCID 2155—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl malonyl chlorideHCID 123460—
SolventDichloromethaneHCID 6344—
SolventOxolane--water (1/1)HCID 21881883—
Product3-Oxo-3-[(1,3-thiazol-2-yl)amino]propanoic acidHCID 1265569969%

Reaction Steps

To a solution of 2-aminothiazole (2.0 g, 19.97 mmol) in dry DCM (30 ml) at 0° C. was added TEA (4.03 g, 2 eq, 39.94 mmol) and methyl 3-chloro-3-oxopropanoate (3.0 g, 1.1 eq, 21.97 mmol). The reaction mixture was stirred for 1 hr at room temperature. The reaction mixture was concentrated to dryness, dissolved in EtOAc and washed well with water. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated. The resultant solid was triturated with Et2O and used directly in the next step with no additional purification (1.1 g, 30% yield). To a solution of the ester 128 (500 mg, 2.49 mmol) in THF/water (1:1, 20 ml) was added LiOH×H2O (209 mg, 2 eq, 4.98 mmol) and the mixture stirred for 2 hrs at room temperature. The mixture was neutralized with 1 M HCl solution and adsorbed onto silica gel. Purification by column chromatography (60% EtOAc in hexanes) afforded the acid 129 as a white solid (320 mg, 69% yield). MS (m/z): 187.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329726B2
Source datasetuspto-grants-2012_12
ORD IDord-131c9df15a4d41ce8e345a3e70050bd5
Source noteuspto-grants-2012_12