HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347619Generated: October 30, 2026
5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chloride → HCID 10182243, compound
https://huagongshe.com/reaction/347619
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chloride | HCID 2735756 | — |
| Reactant | 3-(2-DIMETHYLAMINO-ETHYL)-1H-INDOL-5-YLAMINE | HCID 11820211 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10182243 | HCID 10182243 | 82% |
Reaction Steps
To a solution of 3.05 g (15 mMol) of 5-amino-3-(2-dimethylaminoethyl)-1H-indol in 100 ml of pyridine is added dropwise at ambient temperature a solution of 4.21 g (15 mMol) of 5-chloro-3-methyl-benzo[b]thiophene-2-sulphonyl chloride in 20 ml of pyridine. The reaction mixture is stirred at ambient temperature for 20 hours. It is then evaporated to dryness, slightly alkalinised with diluted ammonia and dissolved in ethyl acetate. The organic phase is washed with water and a saturated solution of sodium bicarbonate, it is separated and dried with anhydrous sodium sulphate. The organic solution is evaporated to dryness and the resulting solid is repeatedly washed with ethyl ether, to yield 5.5 g (82%) of N-[3-(2-dimethylaminoethyl)-1H-indol-5-yl]-5-chloro-3-methyl-benzo[b]thiophene-2-sulphonamide as a solid with m.p.=226–227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176200B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-3d68f9ae31be455ebfea0c0b7d10e94c |
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| Source note | uspto-grants-2007_02 |
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