HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738969Generated: November 1, 2026
1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839916, compound
https://huagongshe.com/reaction/1738969
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Piperidin-4-yl)-1,3-diazinan-2-one | HCID 15572666 | — |
| Reactant | HCID 21839871 | HCID 21839871 | — |
| Product | HCID 21839916 | HCID 21839916 | 176% |
Reaction Steps
3-(3,4-Dichlorophenyl)-3-(5-methoxycarbonyl-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.28 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.126 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 (0.370 g); mp 185-190° C. (d); MS: m/z=573(M+1); NMR(CD3SOCD3): 1.02 (s,1), 1.14 (m,1), 1.69-1.93 (m,5), 3, 14 (s,3), 3.94 (s,3), 4.59 (m,1), 4.79, 4.79 (s,1), 6.6 (d,1, J=8), 6.89 (s,1), 7.16 (d,1, J=81), 7.86 (d,1, J=8), 8.33 (m,2). Analysis for C29H34Cl2N4O4.1.5 H2O.1.0 HCl: Calculated: C, 54.68; H, 6.01, N, 8.80; Found: C, 54.86; H, 5.98; N, 8.89.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965576 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-5ae37aed9be643729873a0102d1f50ff |
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| Source note | uspto-grants-1999_10 |
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