HCID 86754218, compound → SJ-3366

HRID 581864Notes

Reaction equation

HRID 581864 reaction equation
[CH2:1]([C:3]1[C:4](=[O:20])[NH:5][C:6](=[O:19])[NH:7][C:8]=1[C:9](=[O:18])[C:10]1[CH2:11][C:12](=[CH2:17])[CH2:13][C:14](=[CH2:16])[CH:15]=1)[CH3:2].C1(C)C(S(O[CH2:31][CH:32]2[CH2:36][CH:35]=[CH:34][CH2:33]2)(=O)=O)=CC=CC=1>>[CH:32]1([CH2:31][N:7]2[C:8]([C:9](=[O:18])[C:10]3[CH:11]=[C:12]([CH3:17])[CH:13]=[C:14]([CH3:16])[CH:15]=3)=[C:3]([CH2:1][CH3:2])[C:4](=[O:20])[NH:5][C:6]2=[O:19])[CH2:36][CH:35]=[CH:34][CH2:33]1

Participants

3

Reactant 2

HCID 86754218HCID 86754218, compoundHCID 131721305HCID 131721305, compound

Product 1

HCID 474597SJ-3366Yield 59.6%

Procedure

5-Ethyl-6-(3,5-dimethlylbenzoyl)-2,4-pyrimidinedione and (cyclopent-3-en-1-yl)methyl toluenesulfonate were reacted by the same method with the example 1 to obtain the titled compound (84 mg).

Sources & evidence

ORD record
ord-e3d55670d0034646bd509076271c5cb9
Source dataset
uspto-grants-1999_07
Patent number
US05922727

Reaction notes

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