HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514975Generated: November 2, 2026
HCID 66965766, compound → HCID 66965635, compound
https://huagongshe.com/reaction/1514975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66965766 | HCID 66965766 | — |
| Reactant | HCID 86651271 | HCID 86651271 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66965635 | HCID 66965635 | — |
Reaction Steps
A mixture of 3-amino-N-(3,4-dimethylphenyl)-4-hydroxy-benzamide (70 mg) and 2-(4-formyl-3,5-dimethylphenoxy)-N,N-dimethylacetamide (64 mg) in MeOH (5 mL) was stirred at 45° C. for 24 h. The MeOH was removed under reduced pressure and the residue was dissolved in CH2Cl2 (5 mL). To this solution was added DDQ (68 mg) and the dark mixture was stirred at room temperature for 6 h. The majority of the solvent was removed under reduced pressure and EtOAc was added. The solution was washed with NaHCO3 solution and water then was dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using EtOAc/CH2Cl2 (1:2) as eluent to give 2-(4-dimethylcarbamoylmethoxy-2,6-dimethylphenyl)-benzooxazole-5-carboxylic acid (3,4-dimethylphenyl)-amide as a brownish solid, mp=207-209° C.; MS (m/z) 470 (M−1); 1H NMR (DMSO-d6, 400 MHz) δ 10.18 (s, 1H), 8.46 (s, 1H), 8.04 (d, J=10.36 Hz, 1H), 7.90 (d, J=8.34 Hz, 1H), 7.60 (s, 1H), 7.53 (d, J=8.08 Hz, 1H), 7.11 (d, J=8.34 Hz, 1H), 6.83 (s, 2H), 4.89 (s, 2H), 3.02 (s, 3H), 2.87 (s, 3H), 2.27 (s, 6H), 2.24 (s, 3H), 2.21 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222248B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-65b2e232ce1b44bdb3ac2117c1400e63 |
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| Source note | uspto-grants-2012_07 |
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