HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455163Generated: October 31, 2026
Cyclopropanecarbonyl chloride → N-[3-({7-cyano-2-[(cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl}oxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide
https://huagongshe.com/reaction/455163
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | N-{3-[(2-amino-7-cyano-1,3-benzothiazol-6-yl)oxy]phenyl}-3-(1-cyano-1-methylethyl)benzamide | HCID 86644680 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[3-({7-cyano-2-[(cyclopropylcarbonyl)amino]-1,3-benzothiazol-6-yl}oxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide | HCID 59454483 | 69.1% |
Reaction Steps
To a solution of N-{3-[(2-amino-7-cyano-1,3-benzothiazol-6-yl)oxy]phenyl}-3-(1-cyano-1-methylethyl)benzamide (150 mg, 0.33 mmol) in pyridine (2 mL) was added cyclopropanecarbonyl chloride (59 μL, 0.66 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure. The residue was suspended in ethyl acetate (50 mL), washed with 5% aqueous sodium hydrogen carbonate solution (50 mL) and saturated brine (50 mL), successively, and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=30/70→100/0), and the obtained solution was concentrated under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound (119 mg, 69%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497274B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b7bf634920d042f3b1b4b318b914d3e8 |
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| Source note | uspto-grants-2013_07 |
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