Ethyl[(6-methylpyridin-2-yl)methyl]amine → HCID 10391928, compound

HRID 2115474Notes

Reaction equation

HRID 2115474 reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([CH2:24][C:25]([OH:27])=O)[C:15]2[CH:23]=[C:22]3[C:18]([CH:19]=[N:20][NH:21]3)=[CH:17][CH:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:28]([NH:30][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[C:34]([CH3:38])[N:33]=1)[CH3:29]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([C:15]2[CH:23]=[C:22]3[C:18]([CH:19]=[N:20][NH:21]3)=[CH:17][CH:16]=2)[CH2:24][C:25]([N:30]([CH2:28][CH3:29])[CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[C:34]([CH3:38])[N:33]=2)=[O:27])(=[O:12])=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 16495148Ethyl[(6-methylpyridin-2-yl)methyl]amineHCID 58978462[(4-tert-Butyl-benzenesulfonyl)-(1H-indazol-6-yl)-amino]-acetic acid

Product 1

HCID 10391928HCID 10391928, compound

Procedure

prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-(1H-indazol-6-yl)-amino]-acetic acid with ethyl-(6-methyl-pyridin-2-ylmethyl)-amine

Sources & evidence

ORD record
ord-bb6b4c86af064e2f8a5acbe27437eea4
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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