HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504624Generated: October 27, 2026
Dimethylacetamide → N-{2-[5-(hydroxymethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylthiophene-2-sulfonamide
https://huagongshe.com/reaction/504624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 2-Bromopropanedial | HCID 74945 | — |
| Reactant | 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide | HCID 57475960 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-{2-[5-(hydroxymethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylthiophene-2-sulfonamide | HCID 57475965 | 39% |
Reaction Steps
A mixture of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (1.00 g), bromomalonaldehyde (0.86 g) and N,N-dimethylacetamide (8 ml) was stirred at 80° C. for 3 hr. Water was added to the reaction mixture, and the resulting crystals were collected by filtration, washed with water, and dried. The obtained crystals were dissolved in tetrahydrofuran (8 ml) and methanol (8 ml), sodium borohydride (63 mg) was added at 0° C., and the mixture was stirred at 0° C. for 1 hr. The reaction mixture was concentrated, 10% aqueous citric acid solution was added, and the resulting crystals were collected by filtration, washed with water, and dried. The crystals were subjected to silica gel column chromatography to give the title compound (0.43 g, yield 39%) as colorless crystals from a fraction eluted with ethyl acetate-hexane (3:1, volume ratio). melting point 201-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777047B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-f7ad2e9df6f3458db89d493033e02be4 |
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| Source note | uspto-grants-2010_08 |
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