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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652758Generated: November 3, 2026

1-(Cyclopropylmethyl)pyrrolidine-2-methylamine → N-(1-cyclopropylmethyl-2-pyrrolidylmethyl)-2-methoxy-3-isopropyl-5-sulphamoyl-6-methylbenzamide

https://huagongshe.com/reaction/652758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Cyclopropylmethyl)pyrrolidine-2-methylamineHCID 3018274—
Reactant2-Methoxy-3-isopropyl-5-sulphamoyl-6-methylbenzoyl chlorideHCID 20196820—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-(1-cyclopropylmethyl-2-pyrrolidylmethyl)-2-methoxy-3-isopropyl-5-sulphamoyl-6-methylbenzamideHCID 5411455424%

Reaction Conditions

Temperature10 °C

Reaction Steps

4.3 g of 1-cyclopropylmethyl-2-aminomethylpyrrolidine (0.028 mole) and 40 ml of methylethyl ketone are placed in 250 ml flask fitted with an agitator, a thermometer and a dropping funnel. The mixture is cooled to about 10° C. and a solution of 7.6 g of 2-methoxy-3-isopropyl-5-sulphamoyl-6-methyl benzoyl chloride (0.025 mole) in 50 ml of methyl-ethyl-ketone is poured in drop by drop. The mixture is reacted for 1 hour at room temperature then evaporated dry under vacuum, and the residue is dissolved in 100 ml of water and 10 ml of hydrochloric acid (density 1.18). The solution is sucked up under vacuum to eliminate the last traces of solvent, an insoluble component is filtered off and the filtrate is made alkaline with 15 ml of ammonia (density=0.91). The precipitate formed is filtered, washed with water and re-crystallised moist in 50 ml of ethyl acetate. 2.5 g (24%) of product is obtained, melting at about 125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673686
Source datasetuspto-grants-1987_06
ORD IDord-74544cdc71c64ca7bc97c19755769a8d
Source noteuspto-grants-1987_06