HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194749Generated: October 29, 2026
Triethylamine → N-(1-cyclohexylmethyl-2-pyrrolidinyl-methyl)-2,3-dimethoxy-5-sulphamoyl benzamide
https://huagongshe.com/reaction/1194749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2,3-Dimethoxy-5-sulphamoylbenzoic acid | HCID 3017698 | — |
| Reactant | [1-(Cyclohexylmethyl)pyrrolidin-2-yl]methanamine | HCID 21268496 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(1-cyclohexylmethyl-2-pyrrolidinyl-methyl)-2,3-dimethoxy-5-sulphamoyl benzamide | HCID 54427560 | — |
Reaction Steps
26.1 g of 2,3-dimethoxy-5-sulphamoyl-benzoic acid (0.10 mole), 40 ml of water, 200 ml of acetone and 10.1 g of triethylamine (0.10 mole) are placed in 500 ml flask fitted with an agitator, a thermometer and a dropping funnel. The solution is cooled to between 0° and +5° C. and 10.9 g of ethyl chloroformate (0.10 mole) is added drop by drop. It is agitated for 1 hour 30 minutes with the temperature kept at about +5° C., then 19.6 g of 1-cyclohexylmethyl-2 aminomethyl pyrrolidine (0.10 mole) is added drop by drop. A precipitate forms progressively as more and more is added. The reaction medium is then agitated at room temperature, after which it is left to stand. The crystals are filtered, washed three times with water then with 100 ml of 10% ammonia and dried in an oven at 50° C. 50 g is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816471 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-dc3048a1ad3b4b3c95cbc878faf997e2 |
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| Source note | uspto-grants-1989_03 |
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