HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392367Generated: November 3, 2026
1-Aminopiperidine → 5-(4-bromophenyl)-4-(2,4-dichlorophenyl)-N-(1-piperidinyl)thiazole-2-carboxamide
https://huagongshe.com/reaction/1392367
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Aminopiperidine | HCID 16658 | — |
| Reactant | Ethyl 5-(4-bromophenyl)-4-(2,4-dichlorophenyl)thiazole-2-carboxylate | HCID 69288406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(4-bromophenyl)-4-(2,4-dichlorophenyl)-N-(1-piperidinyl)thiazole-2-carboxamide | HCID 69288492 | 78% |
Reaction Steps
Part E: A stirred mixture containing ethyl 5-(4-bromophenyl)-4-(2,4-dichlorophenyl)thiazole-2-carboxylate (1.00 gram, 2.2 mmol) and 1-aminopiperidine (10 mL) is heated overnight at 50° C. The resulting mixture is allowed to attain room temperature, dichloromethane is added and the resulting solution is twice washed with water, dried over MgSO4, filtered and concentrated in vacuo to give an oil. Flash chromatographic purification of this oil (ethyl acetate/petroleum ether=1/3 (v/v)) gives 5-(4-bromophenyl)-4-(2,4-dichlorophenyl)-N-(1-piperidinyl)thiazole-2-carboxamide (870 mg, 78% yield). Melting point: 171-173° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342032B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-0078eca3d0594822937229460eed8269 |
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| Source note | uspto-grants-2008_03 |
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