HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368431Generated: November 2, 2026
N-methyl-2-pyrrolidone → HCID 57513756, compound
https://huagongshe.com/reaction/2368431
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | HCID 13707964 | HCID 13707964 | — |
| Reactant | HCID 57435373 | HCID 57435373 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57513756 | HCID 57513756 | — |
Reaction Steps
To a 5 mL Biotage microwave vial were added NMP (1 ml), 1-benzyl-5-(4-fluorophenyl)-1H-1,2,4-triazol-3-amine (150 mg, 0.559 mmol), 2-(4-fluorophenyl)-4,4-dimethyloxazol-5(4H)-one (116 mg, 0.559 mmol,), under N2. Then it was placed in 100° C. oil bath and stirred for 2.5 h. It was cooled to r.t. and diluted with 2 ml of EtOAc. It was stirred for 10 min that resulted precipitation of the desired product. Then 2 mL of water was added and it was stirred for additional 10 min followed by addition of a couple drops of heptane. The precipitates were collected by filtration and dried under vacuum overnight. This afforded the title compound as a white solid. 1H NMR (400 MHz, DMSO-d6) 1.50 (s, 6H) 5.40 (s, 2H) 7.08-7.14 (m, 2H) 7.24-7.39 (m, 7H) 7.63-7.71 (m, 2H) 7.96-8.04 (m, 2H) 8.33 (s, 1H) 10.17 (s, 1H). MS (m/z) 476.2 M(+1), tR=1.36, Method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703761B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-822f9b5159ba4c1c8611bc2836bb7b1f |
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| Source note | uspto-grants-2014_04 |
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