HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(6-(4-Aminonaphthalen-1-yloxy)pyrimidin-4-yl)-2-methoxy acetamid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Methoxy-N-(6-(4-nitronaphthalen-1-yloxy)pyrimidin-4-yl)acetamide | HCID 70881440 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(6-(4-Aminonaphthalen-1-yloxy)pyrimidin-4-yl)-2-methoxy acetamid | HCID 68229622 | — |
Reaction Steps
A solution of 2-methoxy-N-(6-(4-nitronaphthalen-1-yloxy)pyrimidin-4-yl)acetamide (400 mg, 1.13 mmol) in a mixture of MeOH and DCM and AcOH (2:2:1 v/v/v, 15 mL) was subjected to hydrogenation by passage through a Thales H-cube (1.0 mL min−1, RT, 55 mm CatCart, 10% Pt/C, full hydrogen mode) and was then evaporated in vacuo to afford the title compound, Intermediate M1, as a brown oil (400 mg, 90% purity, 98%); Rt 3.57 min (Method 1 basic); m/z 325 (M+H)+ (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299074B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-ab46738158844652b3d8a7665256c5c2 |
| Source note | uspto-grants-2012_10 |