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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725096Generated: October 30, 2026

1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839920, compound

https://huagongshe.com/reaction/725096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Piperidin-4-yl)-1,3-diazinan-2-oneHCID 15572666—
ReactantHCID 21839931HCID 21839931—
ProductHCID 21839920HCID 21839920122.9%

Reaction Steps

3-(3,4-Dichlorophenyl)-3-(5-ethoxy-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.3 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 (0.28 g); mp 190°-200° C.; MS: m/z=559(M+1); NMR(CDCl3): 1.33 (t,6, J=6.9), 1.71 (m,4), 2.20 (m,2), 2.5 (m,2), 2.74 (broad,1), 3.52 (m,3), 4.04 (m,2), 4.31 (m,1), 4.76 (m,2), 7.05 (m,5), 7.81 (d,1, J=8.41). Analysis for C29H36Cl2N4O3.2.0 HCl.0.5 H2O: Calculated: C, 54.30; H, 6.13, N, 8.73; Found: C, 54.02; H, 6.00; N, 8.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705505
Source datasetuspto-grants-1998_01
ORD IDord-403c35d776b54496b733a0a2512af2f5
Source noteuspto-grants-1998_01