HCID 23302630, compound → HCID 23302285, compound

HRID 1953263Notes

Reaction equation

HRID 1953263 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[S:11]([NH:14][C:15]2[CH:33]=[CH:32][C:18]3[N:19]([CH3:31])[C:20]([NH:22][C:23]4[CH:30]=[CH:29][C:26]([C:27]#[N:28])=[CH:25][CH:24]=4)=[N:21][C:17]=3[CH:16]=2)(=[O:13])=[O:12])[CH:4]=[CH:3][CH:2]=1.[ClH:34].C(=O)([O-])[O-].[NH4+:39].[NH4+]>C(O)C>[ClH:34].[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[S:11]([NH:14][C:15]2[CH:33]=[CH:32][C:18]3[N:19]([CH3:31])[C:20]([NH:22][C:23]4[CH:30]=[CH:29][C:26]([C:27]([NH2:39])=[NH:28])=[CH:25][CH:24]=4)=[N:21][C:17]=3[CH:16]=2)(=[O:12])=[O:13])[CH:4]=[CH:3][CH:2]=1

Participants

4

Procedure

Prepared analogously to Example 1e from 4-[(5-(quinolin-8-yl-sulphonylamino)-1-methyl-1H-benzimidazol-2-yl)-amino]-benzonitrile and hydrochloric acid/ammonium carbonate in ethanol.

Sources & evidence

ORD record
ord-5708a9b7fb734ad4932adb97ff88f349
Source dataset
uspto-grants-2000_09
Patent number
US06114532

Reaction notes

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