HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-3-ylmethanol → 5,11-Dihydro-11-ethyl-2-[3-(hydroxymethyl)piperidin-1-yl]-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Reactant | Dipyridodiazepinone deriv. 15 | HCID 463144 | — |
| Product | 5,11-Dihydro-11-ethyl-2-[3-(hydroxymethyl)piperidin-1-yl]-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 19960019 | — |
Reaction Steps
The title compound, m.p. 194°-197° C., was synthesized from 2-chloro-5,11-dihydro-11l-ethyl-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one and 3-piperidinemethanol using procedures analogous to those described above, except that the mixture was heated at 170°-180° C. for 2.5 hrs, and the product was crystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620974 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-86d277589fbe4f28b104e3eb723a4307 |
| Source note | uspto-grants-1997_04 |