HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330157Generated: October 30, 2026
2-Methylbenzenesulfonamide → HCID 14882520, compound
https://huagongshe.com/reaction/330157
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylbenzenesulfonamide | HCID 6924 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 14882511 | HCID 14882511 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14882520 | HCID 14882520 | 71% |
Reaction Steps
A mixture of E-4-[6-[2-(propylcarbamoyl)vinyl]indol-1-ylmethyl]-3-methoxybenzoic acid (0.76 g), 4-dimethylaminopyridine (0.26 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.41 g), and 2-methylbenzenesulfonamide (0.36 g) in methylene chloride (20 ml) was stirred under an atmosphere of nitrogen for 18 hr. Further quantities of 4-dimethylaminopyridine (0.026 g), the carbodiimide (0.041 g), and the sulfonamide (0.036 g) were added, and stirring was continued for a further 5 hr. The mixture was diluted with methylene chloride (40 ml); washed with 1M hydrochloric acid, water (twice) and brine; dried (MgSO4); and evaporated to give a foam. Crystallization from hot acetonitrile provided the title compound (0.75 g, 71%) as an off-white solid; mp 240°-242°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04894386 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-be9a5c9b8f71428496a293e60c7ccaf2 |
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| Source note | uspto-grants-1990_01 |
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