HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839891, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Piperidin-4-yl)-1,3-diazinan-2-one | HCID 15572666 | — |
| Reactant | HCID 21839947 | HCID 21839947 | — |
| Product | HCID 21839891 | HCID 21839891 | 124.9% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(5-aminocarbonyl-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.2 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.093 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 (0.19 g); mp 240-250° C. (d); MS: m/z=558(M+1); NMR: 2.60-2.77 (m,3), 3.29 (broad,3), 4.67 (m,1), 5.21 (s,1), 6.63 (m,1), 6.85 (s,1), 7.19 (d, J=8, 1), 7.63-7.82 (m,3). Analysis for C27H31Cl2N4O2Br.1.0H2O.1.3HCl.0.2C4H10O: Calculated: 54.16; H, 6.04, N, 10.96; Found: C, 54.21; H, 5.86; N, 10.74.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965576 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-0c4c1570577448dab11c90667dfd1cce |
| Source note | uspto-grants-1999_10 |