HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178502000, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178501999 | HCID 178501999 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178502000 | HCID 178502000 | 80.2% |
Reaction Steps
To a solution of 7-amino-5-(methoxycarbonyl)amino-2-(4-bromophenyl)-1H-benzo[d]-imidazole (60 mg, 0.17 mmol) in dichloromethane (5 mL) was added acetic anhydride (18 mg, 0.17 mmol) and the solution was stirred at room temperature for 3 h. The reaction mixture was concentrated in vacuo and purified by column chromatography on silica gel using hexane/EtOAc (4/1) as the eluant to afford the desired product (55 mg, 80%) as a pale yellow powder: 1H-NMR (300 MHz, CD3OD) δ 2.24 (s, 3H), 3.74 (s, 3H), 7.65 (m, 3H), 7.67 (bs, 1H), 7.90 (m, 2H); ESI MS m/z 403.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232410B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-135b26e731ad45a9882789d8a44d46c3 |
| Source note | uspto-grants-2012_07 |