HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 69462682, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 69463018 | HCID 69463018 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69462682 | HCID 69462682 | 70% |
Reaction Steps
To a solution of 40 mg (0.09 mmol) of 7,8-dimethoxy-1-ethyl-3-(2-aminobenzyl)-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one IIca, add 18.4 mg (0.23 mmol) of pyridine in 4 ml of CH2Cl2, 11.5 mg (0.11 mmol) of acetic anhydride dropwise. Stir for 24 hours. Evaporate to dryness and purify by silica chromatography (AcOEt then AcOEt 5/CH2Cl2 4/EtOH 1). Yield: 70%. M: 144–145° C. 1H-NMR (CDCl3, 300 MHz): d 0.89–0.96 (m, 3H, CH3), 2.01 (s, 1H, COCH3), 3.36–3.45 (m, 2H, CHCH2), 3.61 (s, 3H, OCH3), 3.73–3.84 (m, 2H, CHCH2+1HNCH2), 3.91 (s, 3H, OCH3), 6.60 (s, 1H Ar), 7.07–7.61 (m, 10H Ar). Mass: (M+H)+=472.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250410B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-1d97fc1e88b543e193b7b8df27830902 |
| Source note | uspto-grants-2007_07 |