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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725098Generated: October 29, 2026

1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839756, compound

https://huagongshe.com/reaction/725098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Piperidin-4-yl)-1,3-diazinan-2-oneHCID 15572666—
ReactantHCID 21839908HCID 21839908—
ProductHCID 21839756HCID 21839756142.8%

Reaction Steps

3-(3,4-Dichlorophenyl)-3-(5-fluoro-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.27 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 (0.3 g); mp 180°-205° C. (d); MS: m/z=533(M+1); NMR(CD3 SOCD3): 1.73 (m,4), 2.17 (broad,2), 2.5 (broad,2), 2.74 (broad,1), 3.49 (m,5),3.69 (m,1), 4.36 (m,1), 4.86 (d,1, J=3.3), 6.75 (d,1, J=8.2) 7.07 (s,1), 7.35 (m,3), 7.92 (m,1). Analysis for C27H31 Cl2N4O4F.2.0 HCl: Calculated: C, 53.48; H, 5.49, N, 9.24; Found: C, 53.15; H, 5.53; N, 9.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705505
Source datasetuspto-grants-1998_01
ORD IDord-06911a4aa10b4f63ba805caaf4a01087
Source noteuspto-grants-1998_01