HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-(1-cycloheptylmethyl-2-pyrrolidinylmethyl)-2,3-dimethoxy-5-sulphamoyl benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2,3-Dimethoxy-5-sulphamoylbenzoic acid | HCID 3017698 | — |
| Reactant | 1-Cycloheptylmethyl-2-aminomethylpyrrolidine | HCID 54234427 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(1-cycloheptylmethyl-2-pyrrolidinylmethyl)-2,3-dimethoxy-5-sulphamoyl benzamide | HCID 53910372 | — |
Reaction Steps
13 g of 2,3-dimethoxy-5-sulphamoyl benzoic acid, 150 ml of acetone, 28 ml of water and 7 ml of triethylamine (density 0.726) are placed in a 250 ml flask fitted with an agitator, a thermometer, a condenser and a dropping funnel. The resultant solution is cooled from 0° to +5° C. 5.4 g of ethyl chloroformate is added drop by drop and the reaction medium is agitated for 45 minutes at room temperature and cooled to 0° C. again. 13.7 g of 1-cycloheptylmethyl-2-aminomethylpyrrolidine is added drop by drop. The medium is agitated for 1 hour at room temperature then left to stand. The crystals formed are drained, washed with water and dried in an oven at 30° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04673686 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-2a555d57a26646dfb16cba25986c41a9 |
| Source note | uspto-grants-1987_06 |