HCID 16116212, compound → HCID 10312695, compound

HRID 2237084Notes

Reaction equation

[NH2:1][CH2:2][CH2:3][C:4]1[N:5]([CH:27]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:6]2[C:11]([C:12]=1[CH2:13][CH2:14][O:15][C:16]1[CH:25]=[CH:24][C:19]([C:20]([O:22]C)=[O:21])=[CH:18][CH:17]=1)=[CH:10][C:9]([Cl:26])=[CH:8][CH:7]=2.[Cl:40][C:41]1[CH:46]=[CH:45][C:44]([CH2:47][S:48](Cl)(=[O:50])=[O:49])=[C:43]([N+:52]([O-:54])=[O:53])[CH:42]=1>>[CH:27]([N:5]1[C:6]2[C:11](=[CH:10][C:9]([Cl:26])=[CH:8][CH:7]=2)[C:12]([CH2:13][CH2:14][O:15][C:16]2[CH:25]=[CH:24][C:19]([C:20]([OH:22])=[O:21])=[CH:18][CH:17]=2)=[C:4]1[CH2:3][CH2:2][NH:1][S:48]([CH2:47][C:44]1[CH:45]=[CH:46][C:41]([Cl:40])=[CH:42][C:43]=1[N+:52]([O-:54])=[O:53])(=[O:50])=[O:49])([C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)[C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1

Participants

Reactant 2

HCID 16116212HCID 16116212, compound

HCID 62100059HCID 62100059, compound

Product 1

HCID 10312695HCID 10312695, compoundYield 74%

Procedure

To the methyl 4-{2-[2-(2-aminoethyl)-1-benzhydryl-5-chloro-1H-indol-3-yl]ethoxy}benzoate (Step 6, Example 1)was added (4-chloro-2-nitro-phenyl)-methanesulfonyl chloride according to the procedure in Example 1 Step 7 to generate the product in 74% yield.

Sources & evidence

ORD record: ord-6d5114fcada44e9e8cc4f15d3dc19660
Source dataset: uspto-grants-2010_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07713964B2

Reaction notes

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