HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624961Generated: October 27, 2026
Nitrogen mustard hydrochloride → HCID 178480776, compound
https://huagongshe.com/reaction/1624961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen mustard hydrochloride | HCID 5935 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178508056 | HCID 178508056 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178480776 | HCID 178480776 | 19.8% |
Reaction Steps
Bis(2-chloroethyl)methylamine hydrochloride (97 mg; 0.5 mmol) was added to a stirred solution of 4-amino-1H-pyrazole-3-carboxylic acid (4-fluoro-phenyl)-amide (100 mg; 0.45 mmol), tetrabutylammonium iodide (20 mg; 0.045 mmol) and diisopropyethylamine (200 ul) 1.13 mmol) in DMF (5 ml), and the resulting mixture was heated at 200° C. (100 W) for 30 minutes in a CEM Discover™ microwave synthesiser. The DMF was removed under vacuum, then purified by flash column chromatography, eluting with dichloromethane/methanol/acetic acid/water (90:18:3:2). Product containing fractions were combined and evaporated, treated with HCl in ethyl acetate and then re-evaporated with toluene (2×20 ml) to give an off white solid (27 mg). (LC/MS: Rt 1.64, [M+H]+ 378).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779147B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-b0e5f2ede5e24465a4f0204e5dd31b31 |
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| Source note | uspto-grants-2014_07 |
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