HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904383Generated: November 3, 2026
N-methyl-2-pyrrolidone → HCID 14450289, compound
https://huagongshe.com/reaction/1904383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | HCID 14450287 | HCID 14450287 | — |
| Product | HCID 14450289 | HCID 14450289 | — |
Reaction Steps
To a stirred solution of 1-(4-amino-3-bromo-5-trifluoromethylphenyl)-2,4-dimethylimidazole (4.61 g) in 1-methyl-2-pyrrolidone (50 cm3) was added cuprous cyanide (3.7 g) and the mixture was heated at 150° for 2 days. The mixture was then cooled and the solvent evaporated in vacuo. A solution of ammonia in water (100 cm3 s.g. 0.88) was added and the aqueous phase was extracted with chloroform:methanol, 20:1 (3×100 cm3). The combined organic extracts were dried (MgSO4), filtered and evaporated. The residue was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with chloroform: methanol, 50:1. Combination and evaporation of appropriate fractions gave a solid which was recrystallised from methanol/ethyl acetate to give microcrystals of 1-(4-amino-3-cyano-5-trifluoromethylphenyl)2,4-dimethylimidazole, (1.1 g), m.p. 208°-10°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837334 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-7c4e569a85094e1680142a7c86d03da3 |
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| Source note | uspto-grants-1989_06 |
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