HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867253Generated: October 30, 2026
Toluene → 8-Fluoro-N-methoxy-N-methyl-3-phenyl-3a,4-dihydro-3H-pyrazolo[5,1-c][1,4]-benzoxazine-2-carboxamide
https://huagongshe.com/reaction/1867253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 8-Fluoro-3-phenyl-3a,4-dihydro-3H-pyrazolo(5,1-c)(1,4)benzoxazine 2-ethylcarboxylate | HCID 86624790 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Fluoro-N-methoxy-N-methyl-3-phenyl-3a,4-dihydro-3H-pyrazolo[5,1-c][1,4]-benzoxazine-2-carboxamide | HCID 73045539 | — |
Reaction Steps
A suspension of N-methylmethoxyamine hydrochloride (0.048 g, 0.485 mmol) in dichloromethane (6 mL) at 0° C. was treated with a solution of trimethylaluminum (0.48 mL of a 2.0 M soln in PhMe, 0.971 mmol) and stirred for 20 min. A solution of racemic ester (1-6) (0.150 g, 0.441 mmol) in dichloromethane (2 mL) was added. After stirring for 48 h, the reaction was quenched by the addition of satd. aq. NH4Cl and extracted with EtOAc (2×50 mL). The organic solution was dried over MgSO4, filtered, and concentrated. The residue was purified by flash chromatography (SiO2, 25% EtOAc/hexanes) to provide desired amide (1-7) as a racemic mixture. 1HNMR (500 MHz, CDCl3) δ 7.33-7.35 (m, 4H), 7.17 (m, 1H), 7.10 (m, 1H), 6.80-6.77 (m, 1H), 6.54 (m, 1H), 4.98 (d, J=12.2 Hz, 1H), 4.38 (m, 1H), 3.86-3.82 (m, 4H), 3.30 (br s, 1H) 2.04 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632833B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-5a9ad0b06a554460bcbbbc36f0527dba |
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| Source note | uspto-grants-2009_12 |
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