HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 86676747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 71253070 | HCID 71253070 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86676747 | HCID 86676747 | — |
Reaction Steps
A solution of N-(4-((4-nitronaphthalen-1-yl)oxy)pyridin-2-yl)morpholine-4-carboxamide (900 mg, 2.3 mmol) in a mixture of MeOH (140 mL), DCM (140 mL) and AcOH (4 drops) was subjected to hydrogenation by passage through a Thales H-cube (1.0 mL min−1, 25° C., 55 mm, 10% Pt—C Cat-Cart, full hydrogen mode). The reaction mixture was evaporated in vacuo and the residue was partitioned between DCM (50 mL) and saturated aq. NaHCO3 (20 mL). The organic phase was separated and was washed with brine (20 mL), and then dried and evaporated in vacuo to afford the title compound, Intermediate D5, as a brown solid (0.78 g, 90%); Rt 3.65 min (Method 1 basic); m/z 365 (M+H)+ (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024041B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-eef468fab8f54c13b584e14f1a2b648d |
| Source note | uspto-grants-2015_05 |