HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290586Generated: October 26, 2026
Water → N-(1-isobutyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide
https://huagongshe.com/reaction/2290586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylate | HCID 13420574 | — |
| Reactant | [1-(2-Methylpropyl)pyrrolidin-2-yl]methanamine | HCID 14709035 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | N-(1-isobutyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide | HCID 13420581 | — |
Reaction Steps
A suspension of 5.2 g of methyl 2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxylate and 4.5 g of 1-isobutyl-2-aminomethylpyrrolidine in 20 ml of diethylene glycol is heated at 130°-140° C. and stirred for 18-19 hours. The reaction solution is cooled to room temperature and poured into 150-200 ml of water while stirring. Under ice-cooling crystals are deposited thoroughly and collected by suction filtration. The crude crystals are washed with cold water, dissolved in chloroform and separated on a column of silica gel (developing solvent: methanol/chloroform=1/9). Crystals obtained are recrystallized from about 35 ml of methanol to give crystals of N-(1-isobutyl-2-pyrrolidinylmethyl)-2-methyl-5-sulfamoyl-2,3-dihydrobenzofuran-7-carboxamide, m.p. 182°-184° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04617314 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-5afa806ec4f44f17b8a70f45c2ae6c65 |
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| Source note | uspto-grants-1986_10 |
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