Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652782Generated: October 30, 2026

Acetone → HCID 20196839, compound

https://huagongshe.com/reaction/652782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantIsobutyl chloroformateHCID 62365—
Reactant2,3-Dimethoxy-5-sulphamoylbenzoic acidHCID 3017698—
Reactant1-(Cyclohexylmethyl)pyrrolidin-3-amineHCID 21890640—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 20196839HCID 2019683953.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

7.85 g of 2,3-dimethoxy-5-sulphamoyl benzoic acid, 50 ml of acetone, 10 ml of water and 3 g of triethylamine are placed in a 250 ml flask fitted with an agitator, a thermometer and a dropping funnel. The mixture is cooled to 0° and 4.2 g of isobutyl chloroformate is poured in drop by drop. The mixture is agitated for 45 minutes at 0° C., after which 6 g of 1-cyclohexylmethyl-3-amino-pyrrolidine is dripped in. It is agitated for 2 hours at room temperature, then 80 ml of water is added and the acetone evaporated under vacuum. The product crystallises. It is filtered, washed with water then re-dissolved in 150 ml of water and 20 ml of hydrochloric acid. The solution is filtered with charcoal and the filtrate made alkaline with ammonia. An oil is precipitated and crystallises slowly. The crystals are drained, washed with water and dried in an oven at 50° C. 6.8 g (53%) of product is obtained, with a melting point of 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673686
Source datasetuspto-grants-1987_06
ORD IDord-f66148cd24c24ee390b1d08d985717ed
Source noteuspto-grants-1987_06