HCID 21697621, compound → HCID 21697594, compound

HRID 379486Notes

Reaction equation

[CH3:1][N:2]([CH2:18][CH:19]([C:26]1[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=1)[CH2:20][CH2:21]S(C)(=O)=O)[C:3](=[O:17])[C:4]1[CH:9]=[C:8]([CH:10]2[CH:14]=[N:13][N:12]=[N:11]2)[CH:7]=[CH:6][C:5]=1[O:15][CH3:16].I.[N:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[CH2:40][N:41]1[C:45]2[CH:46]=[CH:47][CH:48]=[CH:49][C:44]=2[N:43]=[C:42]1[C:50]([CH:52]1[CH2:57][CH2:56][NH:55][CH2:54][CH2:53]1)=[O:51]>>[CH3:1][N:2]([CH2:18][CH:19]([C:26]1[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=1)[CH2:20][CH2:21][N:55]1[CH2:56][CH2:57][CH:52]([C:50]([C:42]2[N:41]([CH2:40][C:35]3[CH:36]=[CH:37][CH:38]=[CH:39][N:34]=3)[C:45]3[CH:46]=[CH:47][CH:48]=[CH:49][C:44]=3[N:43]=2)=[O:51])[CH2:53][CH2:54]1)[C:3](=[O:17])[C:4]1[CH:9]=[C:8]([CH:10]2[CH:14]=[N:13][N:12]=[N:11]2)[CH:7]=[CH:6][C:5]=1[O:15][CH3:16]

Participants

Reactant 2

HCID 21697621HCID 21697621, compound

HCID 86754909HCID 86754909, compound

Product 1

HCID 21697594HCID 21697594, compound

Procedure

Prepare by the method of Example 1.7 using N-methyl-N-(2-(4-fluorophenyl)-4-methanesulfonylbutyl)-2-methoxy-5-(4H-triazol-4-yl)benzamide and 4-(1-(pyrid-2-ylmethyl)-1H-benzimidazole-2-carbonyl)piperidine hydriodic acid salt to give the title compound.

Sources & evidence

ORD record: ord-13d60ca7a3404b3f82ad3ce64c442658
Source dataset: uspto-grants-2001_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06297259B1

Reaction notes

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