HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296941Generated: October 30, 2026
4-Nitrobenzoyl chloride → N-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamide
https://huagongshe.com/reaction/2296941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide | HCID 9948802 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamide | HCID 9890633 | 79.3% |
Reaction Steps
A solution of 2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide (prepared in Example 3, 63.0 mg, 0.20 mmol) in tetrahydrofuran (10 mL) was treated with N,N-diisopropylethylamine (0.04 mL, 0.24 mmol) and 4-nitro-benzoyl chloride (49.0 mg, 0.26 mmol). The reaction mixture was stirred at 25° C. for 21 h. At this time, the reaction was concentrated in vacuo. The residue was triturated with diethyl ether to afford N-{4-[2-cyclopentyl-1-(thiazol-2-ylcarbamoyl)-ethyl]-phenyl}-4-nitro-benzamide (73.7 mg, 79.3%) as a pale yellow solid: mp 236-238° C.; FAB-HRMS m/e calcd for C24H24N4O4S (M+H)+ 465.1596, found 465.1617.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489485B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-3477d41943c943efa216a409f84f7a0f |
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| Source note | uspto-grants-2002_12 |
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