3-Methoxypropylamine → HCID 22397875, compound

HRID 1070856Notes

Reaction equation

HRID 1070856 reaction equation
CO[C:3](=[O:32])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[N:17]=[C:16]([S:18]([CH2:21][CH2:22][CH3:23])(=[O:20])=[O:19])[N:15]([C:24]3[CH:29]=[CH:28][C:27]([CH3:30])=[CH:26][CH:25]=3)[C:14]=2[CH:31]=1.[CH3:33][O:34][CH2:35][CH2:36][CH2:37][NH2:38]>>[CH3:33][O:34][CH2:35][CH2:36][CH2:37][NH:38][C:3](=[O:32])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[N:17]=[C:16]([S:18]([CH2:21][CH2:22][CH3:23])(=[O:19])=[O:20])[N:15]([C:24]3[CH:25]=[CH:26][C:27]([CH3:30])=[CH:28][CH:29]=3)[C:14]=2[CH:31]=1

Participants

3

Reactant 2

HCID 16723-MethoxypropylamineHCID 10161578HCID 10161578, compound

Product 1

HCID 22397875HCID 22397875, compound

Procedure

100 mg of 6-[[1-(4-methylphenyl)-2-propanesulfonyl-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was reacted with 3-methoxypropylamine according to general operating instructions 4. 105 mg was obtained.

Workup

  1. custom105 mg was obtained

Sources & evidence

ORD record
ord-fcf4b252e7db4857a157350f27149372
Source dataset
uspto-grants-2005_06
Patent number
US06903126B2

Reaction notes

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