HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427343Generated: October 26, 2026
Nitrogen mustard hydrochloride → HCID 18622550, compound
https://huagongshe.com/reaction/427343
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen mustard hydrochloride | HCID 5935 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(morpholinocarbonylphenyl)-8-amino-5-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxamide | HCID 18622495 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 18622550 | HCID 18622550 | 18% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313118B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-914a6e114dcd4eb185ced59f5a4392f2 |
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| Source note | uspto-grants-2001_11 |
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