HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane methanol → HCID 66941742, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 66941845 | HCID 66941845 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66941742 | HCID 66941742 | — |
Reaction Steps
200 mg 5% Rh on aluminium oxide were added to a solution of 800 mg (1.35 m mol) (R)-2-(4-benzyloxy-3-chloro-5-methyl-phenyl)-1-carboxy-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate in 20 mL THF and the suspension was hydrogenated for 12 h at 40° C. and 3000 hPa hydrogen pressure. To complete the reaction the mixture was combined with 5 mL DCM/MeOH (1:1) and hydrogenated for a further 20 h at 40° C. and 3000 hPa. The catalyst was filtered off, the filtrate was evaporated down, the residue was triturated with DIPE, suction filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528129B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-6107acbbb1c541cc9463d9ef7772099c |
| Source note | uspto-grants-2009_05 |