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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427343Generated: October 26, 2026

Nitrogen mustard hydrochloride → HCID 18622550, compound

https://huagongshe.com/reaction/427343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogen mustard hydrochlorideHCID 5935—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(morpholinocarbonylphenyl)-8-amino-5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 18622495—
Solvent1-ButanolHCID 263—
ProductHCID 18622550HCID 1862255018%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of N-(morpholinocarbonylphenyl)-8-amino-5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxamide (280 mg, 0.69 mmol), bis(2-chloroethyl)methyl amine hydrochloride (190 mg, 1.0 mmol) and sodium hydrogen carbonate (84 mg, 1.0 mmol) in n-butanol (20 mL) was heated at 90° C. for 5 h. After cooling, 2 M ammonium hydroxide (10 mL) was added and the mixture was heated at 50° C. for 1 h. The organic phase was evaporated in vacuo and the residue was purified by flash chromatography on a 5 silica gel column using chloroform/ethanol/conc. ammonium hydroxide (90:10:0.5) as eluent to yield 60 mg (18%) of the title compound: EIMS (70 eV) m/z (relative intensity) 492 (50, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313118B1
Source datasetuspto-grants-2001_11
ORD IDord-914a6e114dcd4eb185ced59f5a4392f2
Source noteuspto-grants-2001_11