HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl (+/-)-7-[[bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate → Methyl (+/-)-7-[[bis[2-(4-piperidinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl (+/-)-7-[[bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate | HCID 53801004 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (+/-)-7-[[bis[2-(4-piperidinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate | HCID 54098965 | 179.7% |
Reaction Steps
A mixture of methyl (±)-7-[[bis[2-(4-pyridinyl)ethyl]amino]carbonyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-2-acetate (0.35 g, 0.65 mmole), PtO2 (0.11 g, 0.48 mmole), 1.0 N HCI (1.3 mL, 1.3 mmole), and MeOH (30 mL) was hydrogenated at 45 psi in a Parr apparatus. After 5 h, the reaction mixture was filtered through celite® and concentrated to give the crude title compound (0.6 g) which was used without further purification. MS(ES) m/e 514.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008214 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-0eb7822146364833a57827bfede81407 |
| Source note | uspto-grants-1999_12 |