HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Piperidin-4-yl)-1,3-diazinan-2-one | HCID 15572666 | — |
| Reactant | HCID 21839869 | HCID 21839869 | — |
| Product | HCID 21839893 | HCID 21839893 | 122.7% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(5-hydroxy-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.23 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.136 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 (0.220 g); mp 200°-210° C; MS: m/z=531(M+1); NMR: 1.0 (s,3), 1.99 (s,1), 2.36 (m,2), 2.7 (m,2), 3.26 (s,3),4.65 (s,1), 5.94 (d,1, J=7.7), 7.18-7.41 (m,9), 7.54 (d,1, J=8.31), 7.77 (d, J=7.5). Analysis for C32H35Cl2N3O2.1.0 HCl.1.5 H2O: Calculated: C, 54.51; H, 6.09, N, 9.41; Found: C, 54.82; H, 5.78; N, 9.41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05589489 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-aefa6a84db4d48bebb2897503f984908 |
| Source note | uspto-grants-1996_12 |