Aniline → HCID 57670966, compound

HRID 554811Notes

Reaction equation

HRID 554811 reaction equation
[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][CH2:16][C:17]([NH:19]C2C=CC=CC=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.NC1C=CC=CC=1.[CH2:45](N)[C:46]1[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=1>>[CH2:45]([NH:19][C:17](=[O:18])[CH2:16][CH2:15][N:13]1[CH2:14][CH:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:9](=[O:37])[N:10]([S:27]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[CH:32][CH:31]=2)(=[O:28])=[O:29])[CH2:11][C:12]1=[O:26])[C:46]1[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=1

Participants

4

Reactant 3

HCID 6115AnilineHCID 7504BenzylamineHCID 57671104HCID 57671104, compound

Product 1

HCID 57670966HCID 57670966, compound

Procedure

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

Sources & evidence

ORD record
ord-94e0501642714f5e80c69d99af7c1c30
Source dataset
uspto-grants-2011_11
Patent number
US08049006B2

Reaction notes

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