Benzimidazole → HCID 15025363, compound

HRID 358996

Reaction equation

HRID 358996 reaction equation
Cl[CH2:2]/[CH:3]=[C:4]1/[C:5]2[CH:18]=[C:17]([C:19]([O:21][CH3:22])=[O:20])[CH:16]=[CH:15][C:6]=2[O:7][CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]/1=2.[N:23]1[C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][C:26]=2[NH:25][CH:24]=1>>[CH3:22][O:21][C:19]([C:29]1[CH:30]=[CH:31][C:26]2[N:25]=[CH:24][N:23]([CH2:2]/[CH:3]=[C:4]3/[C:5]4[CH:18]=[C:17]([C:19]([O:21][CH3:22])=[O:20])[CH:16]=[CH:15][C:6]=4[O:7][CH2:8][C:9]4[CH:14]=[CH:13][CH:12]=[CH:11][C:10]/3=4)[C:27]=2[CH:28]=1)=[O:20]

Participants

3

Reactant 2

HCID 5798BenzimidazoleHCID 10448388Methyl (E)-11-(2-chloroethylidene)-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate

Product 1

HCID 15025363HCID 15025363, compound

Procedure

In Examples 27 through 32, the products were prepared using Compound h and corresponding benzimidazole derivatives in a manner similar to Example 26.

Workup

  1. customIn Examples 27 through 32, the products were prepared

Sources & evidence

ORD record
ord-b6a25219a55640f3ab20bf9dd1e477d1
Source dataset
uspto-grants-1991_03
Patent number
US04999363

Linked notes

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