Aniline → HCID 57671113, compound

HRID 1364366Notes

Reaction equation

HRID 1364366 reaction equation
[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][CH2:16][C:17]([NH:19][C:20]2[CH:25]=C[CH:23]=[CH:22][CH:21]=2)=[O:18])[C:12](=[O:26])[CH2:11][N:10]([S:27]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[CH:32][CH:31]=2)(=[O:29])=[O:28])[C:9]1=[O:37])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:38]C1C=CC=CC=1.NC1C=NC=CC=1>>[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][CH2:16][C:17]([NH:19][C:20]2[CH:25]=[N:38][CH:23]=[CH:22][CH:21]=2)=[O:18])[C:12](=[O:26])[CH2:11][N:10]([S:27]([C:30]2[CH:31]=[CH:32][C:33]([Cl:36])=[CH:34][CH:35]=2)(=[O:28])=[O:29])[C:9]1=[O:37])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 6115AnilineHCID 100093-AminopyridineHCID 57671104HCID 57671104, compound

Product 1

HCID 57671113HCID 57671113, compound

Procedure

Instead of the starting material compound of Example 273, that is, aniline, 3-aminopyridine was used for the similar procedure as in Example 273 to obtain the title compound.

Sources & evidence

ORD record
ord-e44a1f269d65490caac5b135dd209089
Source dataset
uspto-grants-2011_02
Patent number
US07888348B2

Reaction notes

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