HCID 10911081, compound → HCID 67668089, compound

HRID 1956275Notes

Reaction equation

HRID 1956275 reaction equation
C1(O[C:8](=[O:20])[NH:9][C:10]2[C:11]([O:18][CH3:19])=[N:12][C:13]([CH3:17])=[C:14]([CH3:16])[CH:15]=2)C=CC=CC=1.[C:21]([O:24][C:25]1[CH:30]=[CH:29][C:28]([N:31]2[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]2)=[CH:27][CH:26]=1)(=[O:23])[CH3:22]>>[CH3:16][C:14]1[CH:15]=[C:10]([NH:9][C:8]([N:34]2[CH2:33][CH2:32][N:31]([C:28]3[CH:27]=[CH:26][C:25]([O:24][C:21](=[O:23])[CH3:22])=[CH:30][CH:29]=3)[CH2:36][CH2:35]2)=[O:20])[C:11]([O:18][CH3:19])=[N:12][C:13]=1[CH3:17]

Participants

3

Reactant 2

HCID 10911081HCID 10911081, compoundHCID 11086894Phenyl N-(5,6-dimethyl-2-methoxypyridin-3-yl)carbamate

Product 1

HCID 67668089HCID 67668089, compoundYield 89%

Procedure

Phenyl-N-(5,6-dimethyl 2methoxypyridin 3-yl)carbamate and 1-(4-acetoxyphenyl)piperazine were reacted by the same way with the example 1 to obtain the titled compound.

Sources & evidence

ORD record
ord-90c690ffe0b749f196ae302468c7f9e1
Source dataset
uspto-grants-1998_07
Patent number
US05780472

Reaction notes

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