HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839776, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Piperidin-4-yl)-1,3-diazinan-2-one | HCID 15572666 | — |
| Reactant | HCID 21839783 | HCID 21839783 | — |
| Product | HCID 21839776 | HCID 21839776 | 151.1% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(6-isopropoxy-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.50 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.225 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 (0.567 g); mp 160°-170° C. (d); MS: m/z=573(M+1); NMR(CD3 SOCD3): 1.38 (m,6), 1.83 (broad,5), 3.29 (s,3), 4.82 (m,1), 6.74-6.97 (m,2), 7.18-7.64 (m,4). Analysis for C30H38Cl2N4 O3.1.0 HCl.1.5 H2O: Calculated: C, 56.56; H, 6.64, N, 8.79; Found: C, 56.49; H, 6.40; N, 8.78.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705505 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-009bb5cb7b4e4808851628f12810d4d3 |
| Source note | uspto-grants-1998_01 |