HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Aminopiperidin-1-yl)ethan-1-one → HCID 21070357, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Aminopiperidin-1-yl)ethan-1-one | HCID 4962477 | — |
| Reactant | HCID 21070559 | HCID 21070559 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21070357 | HCID 21070357 | — |
Reaction Steps
A suspension of (4-amino-2-ethanesulfinyl-pyrimidin-5-yl)-(2-methoxy-5-methyl-phenyl)-methanone (22.3 mg, 0.0698 mmol, Example 325) and 1-(4-amino-piperidin-1-yl)-ethanone (14.9 mg, 0.105 mmol, prepared as described in U.S. Pat. No. 5,817,828) in isopropyl alcohol (2.5 mL) was heated at 120° C. in a sealed tube under microwave conditions for 0.3 to 1 hour. The resulting reaction mixture was evaporated in vacuo and crude product was purified on silica gel with 95:5 of dichloromethane/methanol to give 1-[4-[4-amino-5-(2-methoxy-5-methyl-benzoyl)-pyrimidin-2-ylamino]-piperidin-1-yl]-ethanone as a white solid (23.1 mg). MS (M+H)+, 384.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07615634B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-b213acbd1048480a8102a73ceed2c38a |
| Source note | uspto-grants-2009_11 |