HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267731Generated: November 1, 2026
Triethylamine → 1-(5-Coumaranyl carbonyl)-4-(2-thiazolyl) piperazine
https://huagongshe.com/reaction/267731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Thiazol-2-yl)piperazine | HCID 911806 | — |
| Reactant | 2,3-Dihydro-1-benzofuran-5-carbonyl chloride | HCID 2776153 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Coumaranyl carbonyl)-4-(2-thiazolyl) piperazine | HCID 39106923 | 76.3% |
Reaction Steps
To a solution of 9 g of 1-(2-thiazolyl) piperazine and 5 g of anhydrous triethylamine in 200 ml of anhydrous tetrahydroduran, there were added dropwise, a solution of 9.1 g of 5-coumaranyl carboxylic acid chloride in 20 ml of tetrahydrofuran. After the completion of the addition, the reaction mixture was heated at 60° C for two hours, then, the so-formed precipitate was suction-filtered off. The filtrate was evaporated under reduced pressure and the crystalline residue was washed with water then recrystallized in 70 ml of ethanol. There were obtained 12 g of 1-(5-coumaranyl carbonyl)-4-(2-thiazolyl) piperazine, melting (K) at 150°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03944551 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-b763e8445bf2457c9c8413ea56394967 |
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| Source note | uspto-grants-1976_03 |
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