HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944701Generated: October 30, 2026
Triethylamine → 3-Chloropropane-1-sulfonic acid [2-(4-cyclopropyl-piperazin-1-yl)benzooxazol-5-ylmethyl]amide
https://huagongshe.com/reaction/1944701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | 2-(4-Cyclopropylpiperazin-1-yl)benzooxazole | HCID 47453664 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloropropane-1-sulfonic acid [2-(4-cyclopropyl-piperazin-1-yl)benzooxazol-5-ylmethyl]amide | HCID 59588792 | 42% |
Reaction Steps
To a solution of 5-aminomethyl-[2-(4-cyclopropylpiperazin-1-yl)benzooxazole (500 mg, 1.84 mmol) in CH2Cl2 (15 mL) was added Et3N (929 mg, 9.2 mmol). The mixture was stirred at 0° C. for 5 min and then 3-chloropropane-1-sulfonyl chloride (326 mg, 1.84 mmol) was added dropwise. The mixture was stirred at 0° C. for 1 h and brought gradually to rt. Then the mixture was stirred for another 1 h. The volatiles were removed and the residue was extracted with CH2Cl2. The resulting residue was purified by column chromatography on silica gel (elute: 5% CH2Cl2 in methanol) to give 3-chloropropane-1-sulfonic acid [2-(4-cyclopropylpiperazin-1-yl)benzooxazol-5-ylmethyl]amide (315 mg, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394842B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-2d193ea6640549a2943880f9ee829a0b |
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| Source note | uspto-grants-2013_03 |
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