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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226317Generated: October 30, 2026

ethyl (2E)-5-chloro-4-oxo-2-pentenoate → ethyl (2E)-3-(2-([1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-1,3-thiazol-4-yl)acrylate

https://huagongshe.com/reaction/226317

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (2E)-5-chloro-4-oxo-2-pentenoateHCID 86603623—
ReactantN-[1-(4-chlorobenzoyl)-3-pyrrolidinyl]thioureaHCID 86603625—
SolventAcetonitrileHCID 6342—
Productethyl (2E)-3-(2-([1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-1,3-thiazol-4-yl)acrylateHCID 8660362487.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

The mixture of ethyl (2E)-5-chloro-4-oxo-2-pentenoate (0.5 g) and N-[1-(4-chlorobenzoyl)-3-pyrrolidinyl]thiourea (0.8 g) in acetonitrile (10 mL) was stirred at 70° C. for 3 hours, and the mixture was evaporated in vacuo. To the residue was added a solution of AcOEt and water, and the mixture was adjusted to pH 8 with 20% aqueous potassium carbonate. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel using AcOEt as an eluent. The eluted fractions containing the desired product were collected and evaporated in vacuo to give ethyl (2E)-3-(2-{[1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-1,3-thiazol-4-yl)acrylate (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-ea2149db57234ea1a23ba2bf900b6b5f
Source noteuspto-grants-2009_07