Dimethylamine → HCID 21097170, compound

HRID 1350813Notes

Reaction equation

[C:1]([C:5]1[CH:6]=[C:7]([NH:36][S:37]([CH3:40])(=[O:39])=[O:38])[C:8]([O:34][CH3:35])=[C:9]([NH:11][C:12](=[O:33])[C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[C:15]([N:20]3[CH:24]=[C:23]([C:25]4[CH:26]=[N:27][C:28]([CH:31]=[CH2:32])=[CH:29][CH:30]=4)[N:22]=[N:21]3)[CH:14]=2)[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:41][NH:42][CH3:43]>>[C:1]([C:5]1[CH:6]=[C:7]([NH:36][S:37]([CH3:40])(=[O:38])=[O:39])[C:8]([O:34][CH3:35])=[C:9]([NH:11][C:12](=[O:33])[C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[C:15]([N:20]3[CH:24]=[C:23]([C:25]4[CH:26]=[N:27][C:28]([CH2:31][CH2:32][N:42]([CH3:43])[CH3:41])=[CH:29][CH:30]=4)[N:22]=[N:21]3)[CH:14]=2)[CH:10]=1)([CH3:2])([CH3:3])[CH3:4]

Participants

Reactant 2

HCID 674Dimethylamine

HCID 21097370HCID 21097370, compound

Product 1

HCID 21097170HCID 21097170, compound

Procedure

Example 163 was prepared from N-(5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-4-methyl-3-[4-(6-vinyl-pyridin-3-yl)-1,2,3-triazol-1-yl]-benzamide (Example 151) and dimethylamine in the same manner as Example 151. ESI MS m/z 606 [C31H39N7O4S+H]+.

Sources & evidence

ORD record: ord-37a52b91287940239fa7733f9f1ca83c
Source dataset: uspto-grants-2007_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07214802B2

Reaction notes

Loading…