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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285441Generated: October 30, 2026

Hydrochloric Acid → 6-{1-Hydroxy-4-[bis-chloroethyl-amino]butyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1285441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant6-{1-Oxo-4-[di-(2-chloroethyl)-amino]butyl}-3,4-dihydrocarbostyrilHCID 20229420—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-{1-Hydroxy-4-[bis-chloroethyl-amino]butyl}-3,4-dihydrocarbostyrilHCID 20229456—

Reaction Steps

2.5 Grams of 6-{1-oxo-4-[di-(2-chloroethyl)-amino]butyl}-3,4-dihydrocarbostyril was dissolved in 80 ml of methanol, with stirring at a room temperature condition 1.6 g of sodium borohydride was added gradually to the mixture in 15 minutes and further stirred at a room temperature for 2 hours. To the reaction mixture was added 5 ml of concentrated hydrochloric acid was added and the reaction mixture was concentrated under a reduced pressure to dryness. The residue thus obtained was dissolved in 10 ml of water, the pH of the solution was adjusted to 6-7 by adding 2N-sodium hydroxide aqueous solution and stirred to precipitate crystals. The crystals were collected by filtration washed with water and dried to obtain 1.4 g of 6-{1-hydroxy-4-[bis(2-chloroethyl)amino]-butyl}-3,4-dihydrocarbostyril in colorless powdery product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567187
Source datasetuspto-grants-1986_01
ORD IDord-382d5b18491a49d0a5dc794474c55aed
Source noteuspto-grants-1986_01