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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291950Generated: October 30, 2026

Ammonium Acetate → 1-(5-Isoquinolinesulfonyl)-3-amino-5-methylpyrrolidine

https://huagongshe.com/reaction/2291950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(5-Isoquinolinesulfonyl)-5-methyl-3-pyrrolidoneHCID 14326857—
SolventMethanolHCID 887—
Product1-(5-Isoquinolinesulfonyl)-3-amino-5-methylpyrrolidineHCID 14326858—

Reaction Conditions

Temperature20 °C

Reaction Steps

To 30 ml of methanol were added 1.45 g of the thus obtained 1-(5-isoquinolinesulfonyl)-5-methyl-3-pyrrolidone, 0.39 g of ammonium acetate and 0.32 g of sodium cyanoborohydride, followed by stirring at 20° C. for 24 hours. The methanol was removed under reduced pressure, and 100 ml of chloroform was added to the resultant product. Then, the mixture was washed twice with 50 ml each of water, washed once with 50 ml of a 50% aqueous sodium hydrogencarbonate solution, and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to obtain a residue. The residue thus obtained was subjected to purification by silica gel column chromatography (Wacogel C200, 50 g; solvent: chloroform) to obtain 0.96 g of 1-(5-isoquinolinesulfonyl)-3-amino-5-methylpyrrolidine [Compound (77)]. Compound (77) was analyzed to give the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798897
Source datasetuspto-grants-1989_01
ORD IDord-dd81f3dd37d142b6864e04860a94257f
Source noteuspto-grants-1989_01