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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291952Generated: October 31, 2026

Sodium Hydroxide → HCID 14257567, compound

https://huagongshe.com/reaction/2291952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 14257566HCID 14257566—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 14257567HCID 14257567—

Reaction Steps

To 75 ml of an anhydrous methanol solution containing 5.89 g of the thus obtained N-acetonyl-N-hexyl-5-isoquinolinesulfonamide were added 13.03 g of ammonium acetate and 0.75 g of sodium cyanoborohydride, followed by stirring at 15° to 20° C. for 19 hours. Then, the methanol was removed at 30° C. under reduced pressure. To the resultant reaction product were added 50 ml of chloroform and 50 ml of 1N sodium hydroxide solution. The chloroform layer was dried with anhydrous magnesium sulfate, and the chloroform was removed under reduced pressure to obtain a residue. The residue thus obtained was subjected to purification by silica gel column chromatography (Wacogel C-200, 100 g; solvent: chloroform) to obtain 2.75 g of N-(2-aminopropyl)-N-hexyl-5-isoquinolinesulfonamide [Compound (11)]. Compound (11) was analyzed to give the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798897
Source datasetuspto-grants-1989_01
ORD IDord-967116a071bc4e9d92a4bef28f294382
Source noteuspto-grants-1989_01