HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Piperidin-4-yl)-1,3-diazinan-2-one | HCID 15572666 | — |
| Reactant | HCID 21839833 | HCID 21839833 | — |
| Product | HCID 21839992 | HCID 21839992 | 95.1% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(5-acetoxy-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.35 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.135 g) by a method similar to that described in Example 8. The reaction product was not purified by chromatography but converted to the corresponding hydrochloride salt as described in the Example 8 to afford the title compound (0.25 g); mp 190°-200° C.; MS: m/z=573(M+1); NMR(CD3SOCD3): 1.63 (broad,6), 2.14 (broad,3), 2.27 (s,3), 2.7 (broad,1), 3.6 (m,3), 4.22 (m,1), 4.85 (d,1, J=3.6), 7.09 (m,5), 7.95 (d,1 J=8.2). Analysis for C29H34Cl2N4O4.2.0 HCl.1.0 H2O: Calculated: C, 52.42; H, 5.76, N, 8.43; Found: C, 52.83; H, 5.58; N, 8.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705505 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-b1964f8947f04b8888de5327a296dc2a |
| Source note | uspto-grants-1998_01 |