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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082229Generated: October 31, 2026

1-(Piperidin-4-yl)-1,3-diazinan-2-one → HCID 21839912, compound

https://huagongshe.com/reaction/1082229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Piperidin-4-yl)-1,3-diazinan-2-oneHCID 15572666—
ReactantHCID 21839764HCID 21839764—
ProductHCID 21839912HCID 21839912145.7%

Reaction Steps

3-(3,4-Dichlorophenyl)-3-(4,5,6,7-tetrafluoro-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)propionaldehyde (0.43 g) was coupled to 4-(2-oxoperhydropyrimidine-1-yl)piperidine (0.183 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 desired 3-[1-(3,4-Dichlorophenyl)-3-(4-(2-oxoperhydropyrimidine-1-yl)piperidino)propyl]-2-methyl-2,3-dihydro-4,5,6,7-terafluoro-isoindol-1-one hydrochloride (0.465 g); mp 220° C. (d); MS: m/z=587(M+1); NMR: 1.18 (m, 4), 2.67 (m, 4), 3.36 (s,3), 4.58 (m, 1), 4.90 (s,1), 6.87-7.37 (m,3). Analysis for C27H28Cl2N4O2F4 ·1.5.HCl·2H2O: Calculated: C, 47.82; H, 4.98, N, 8.26; Found: C, 48.15; H, 4.73; N, 7.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589489
Source datasetuspto-grants-1996_12
ORD IDord-6415b96bf4744a2eaac52b1c96d6ecd3
Source noteuspto-grants-1996_12