HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773679Generated: November 1, 2026
HCID 117601614, compound → HCID 117601434, compound
https://huagongshe.com/reaction/1773679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 117601614 | HCID 117601614 | — |
| Reactant | HCID 178478979 | HCID 178478979 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117601434 | HCID 117601434 | — |
Reaction Steps
Tert-butyl 6-(3,5-dimethylisoxazol-4-yl)-2-ethoxy-4-(methoxy(methyl)carbamoyl)-1H-benzo[d]imidazole-1-carboxylate was dissolved in THF (3 mL). To the solution was added a solution of phenyl magnesium chloride (2M in THF, 0.508 mmol, 0.254 mmol) at −78° C. after the addition, the reaction was allowed to warm up to room temperature. The reaction was stirred for 17 hat the same temperature. The reaction mixture was quenched with water (30 mL). The whole was extracted with AcOEt (30 mL×3). Organic layer was washed with brine (30 mL) and dried over Na2SO4. The solvent was removed under a reduced pressure to give the crude product. The crude product was purified by a silica gel column chromatography (hexane:EtOAc, 7:1 to 3:1) to give tert-butyl 4-benzoyl-6-(3,5-dimethylisoxazol-4-yl)-2-ethoxy-1H-benzo[d]imidazole-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255089B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-f7049a52f6614508a13b1bbec18c446b |
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| Source note | uspto-grants-2016_02 |
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