HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582142Generated: October 26, 2026
4-Fluorobenzoyl chloride → N-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamide
https://huagongshe.com/reaction/1582142
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-Cyclohexyl-4-methoxy-benzothiazol-2-ylamine | HCID 22719574 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamide | HCID 9952034 | 14% |
Reaction Steps
To a solution of 0.05 g (0.19 mMol) 7-cyclohexyl-4-methoxy-benzothiazol-2-ylamine in 2 ml THF were added 0.1 ml ethyl diisopropyl amine and 0.027 ml (0.23 mMol) 4-fluoro-benzoyl chloride. The reaction mixture was heated to 70° C. for 2 h. The solvent was evaporated to dryness, the residue taken up in dichloro methane and washed with water and brine. The organic phase was dried over sodium sulfate and evaporated to dryness in vacuo. The residue was subjected to column chromatography (ethyl acetate/hexane 1:9, 1:4) to yield 0.01 g (14%) of N-(7-cyclohexyl-4-methoxy-benzothiazol-2-yl)-4-fluoro-benzamide as a light yellow solid; F.p.: 192-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06734179B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-d6d6fc2e4af94ca5b8ce9d321944528c |
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| Source note | uspto-grants-2004_05 |
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