HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391273Generated: October 30, 2026
2-Aminothiazole → HCID 44234337, compound
https://huagongshe.com/reaction/391273
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | HCID 66841714 | HCID 66841714 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 44234337 | HCID 44234337 | 7% |
Reaction Steps
8-Fluoro-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-4-carboxylic acid methyl ester (0.6 mmol) and 2-aminothiazol (0.6 mmol) were dissolved in 2.5 ml xylene. Reaction was performed by microwave irradiation for 30 minutes at 140° C. The solution obtained from this reaction was cooled to room temperature and extracted by 2 mol/l hydrochloric acid and ethyl acetate. The ethyl acetate extract was dried over sodiumsulfate and the solvent removed in vacuo. After evaporation of the solvent in vacuo 8-Fluoro-5-oxo-2,3,4,5-tetrahydro-benzo[b]oxepine-4-carboxylic acid thiazol-2-ylamide was obtained as a white powder in a yield of 7%. LC-MS: 1.9 min, 307.0 (MH+) 1H-NMR: (DMSO-d6, 500 MHz): d [ppm]: 12.102 (s, 1H), 7.731 (t, 1H, J=7.3 Hz), 7.464 (d, 1H, J=3.2 Hz), 7.234 (d, 1H, J=3.6 Hz), 7.056 (m, 2H, J=7.8 Hz), 4.654 (m, 1H, J=2.6 Hz), 4.340 (m, 1H, J=7.6 Hz), 4.013 (m, 1H, J=7.2 Hz), 2.502 (m, 2H, J=1.8 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383838B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-e0810f31c24649a4af64b8052ba3e8e6 |
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| Source note | uspto-grants-2013_02 |
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