Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2,3-Dimethoxy-5-sulphamoylbenzoic acid | HCID 3017698 | — |
| Reactant | HCID 21268519 | HCID 21268519 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70428452 | HCID 70428452 | — |
Reaction Steps
13 g of 2,3-dimethoxy-5-sulphamoyl-benzoic acid (0.05 mole), 150 ml of acetone, 35 ml of water and 5 g of triethylamine (0.05 mole) are placed in a 500 ml flask fitted with an agitator, a thermometer, a condenser and a droping funnel. The mixture is cooled to between 0° to +5° C. and 5.5 g of ethyl chloroformate (0.05 mole) is poured in drop by drop. The reaction medium is agitated until the precipitate is completely dissolved, then re-cooled to 0° C. and 9.7 g of 1-(1-cyclohexenyl)-methyl-2-aminomethyl-pyrrolidine (0.05 mole) is poured in drop by drop.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673686 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-be4d0d0a0c2345bdbe28c34b79fee8dd |
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| Source note | uspto-grants-1987_06 |
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