Ethanol, 2-((2-pyridinylmethyl)amino)- → HCID 9984312, compound

HRID 2115482Notes

Reaction equation

HRID 2115482 reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([CH2:24][C:25](O)=[O:26])[C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N:21]([CH3:23])[CH3:22])[CH:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[N:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1[CH2:34][NH:35][CH2:36][CH2:37][OH:38]>>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([S:11]([N:14]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N:21]([CH3:22])[CH3:23])[CH:16]=2)[CH2:24][C:25]([N:35]([CH2:36][CH2:37][OH:38])[CH2:34][C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][N:28]=2)=[O:26])(=[O:12])=[O:13])=[CH:9][CH:10]=1)([CH3:3])([CH3:2])[CH3:4]

Participants

3

Reactant 2

HCID 81135Ethanol, 2-((2-pyridinylmethyl)amino)-HCID 58978433[(4-tert-Butyl-benzenesulfonyl)-(3-dimethylamino-phenyl)-amino]-acetic acid

Product 1

HCID 9984312HCID 9984312, compound

Procedure

prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-(3-dimethylamino-phenyl)-amino]-acetic acid with 2-[(pyridin-2-ylmethyl)-amino]-ethanol

Sources & evidence

ORD record
ord-b814465c65d8419e8a96f9904755d7f2
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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