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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2,3-Dimethoxy-5-sulphamoylbenzoic acidHCID 3017698—
Reactant[1-(Cyclohexylmethyl)pyrrolidin-2-yl]methanamineHCID 21268496—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductN-(1-cyclohexylmethyl-2-pyrrolidinyl-methyl)-2,3-dimethoxy-5-sulphamoyl benzamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816471
Source datasetuspto-grants-1989_03
ORD IDord-dc3048a1ad3b4b3c95cbc878faf997e2
Source noteuspto-grants-1989_03