Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21162331 | HCID 21162331 | — |
| Reactant | HCID 178521935 | HCID 178521935 | — |
| Solvent | Water | HCID 962 | — |
| Product | Glisindamide | HCID 3038458 | — |
Reaction Steps
3.6 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfon-amide are carefully mixed with 2.5 g of trichloroacetyl-cyclohexyl amide and 2.8 g of potassium carbonate and the mixture is heated in a bath for 1 hour at 160° C. After cooling, the reaction mixture is treated with water and hydrochloric acid, filtered off with suction and the reaction product is reprecipitated from very dilute ammonia and recrystallized from dilute acetone. The N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl-urea obtained melts at 214°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282239 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-c11ac8e675974bafb761175c8e531b7a |
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| Source note | uspto-grants-1981_08 |
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