HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376002Generated: 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/2376002
Participants
| Role | Name | HCID | Charge |
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| Reactant | ethyl (2E)-5-chloro-4-oxo-2-pentenoate | HCID 86603623 | — |
| Reactant | N-[1-(4-chlorobenzoyl)-3-pyrrolidinyl]thiourea | HCID 86603625 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | ethyl (2E)-3-(2-([1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-1,3-thiazol-4-yl)acrylate | HCID 86603624 | 87.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465731B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-21b9350d2c054392b1bbebeefc86ccd5 |
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| Source note | uspto-grants-2008_12 |
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