HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922286Generated: November 1, 2026
Ethanesulfonyl chloride → HCID 86618572, compound
https://huagongshe.com/reaction/1922286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86618573 | HCID 86618573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86618572 | HCID 86618572 | — |
Reaction Steps
A mixture of (S)-6-methoxy-N-(piperidin-3-yl)benzo[d]thiazol-2-amine hydrochloride salt (2.0 g, 5.95 mmol), ethylsulfonyl chloride (1.13 ml, 11.91 mmol) and DIPEA (4.11 ml, 23.8 mmol) in NMP (25 ml) was heated at 55° C. for 16 hours 50 min. The reaction mixture was allowed to cool down to room temperature and diluted with water (150 ml) and ethyl acetate (150 ml). After stirring vigorously for 1 hour the separated organic layer was washed with water (3×100 ml), saturated sodium bicarbonate solution (3×100 ml), water (100 ml) and brine (100 ml) and dried over sodium sulfate. Concentration in vacuo and purification by flash chromatography over silica gel with ethyl acetate:hexane (20:80-100:0) provided (S)—N-(1-(ethylsulfonyl)piperidin-3-yl)-6-methoxybenzo[d]thiazol-2-amine as tan solid. Yield: 1.22 g. ES/MS m/z 356.0 (MH+), Rt=2.12 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173689B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-9ceab0e1cd584173854fd8164bf7762a |
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| Source note | uspto-grants-2012_05 |
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