HCID 67238446, compound → HCID 67239844, compound

HRID 2170888Notes

Reaction equation

HRID 2170888 reaction equation
[Cl:1][C:2]1[C:3]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:4][N:5]([C:7]2[N:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([OH:11])=O)[CH:6]=1.[Cl-].[CH2:23]([O:25][C:26](=[O:38])[CH:27]([OH:37])[CH:28]([NH3+:36])[CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[CH3:24]>>[Cl:1][C:2]1[C:3]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:4][N:5]([C:7]2[N:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([NH:36][CH:28]([CH2:29][C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=2)[CH:27]([OH:37])[C:26]([O:25][CH2:23][CH3:24])=[O:38])=[O:11])[CH:6]=1

Participants

3

Reactant 2

HCID 67238446HCID 67238446, compoundHCID 86644788HCID 86644788, compound

Product 1

HCID 67239844HCID 67239844, compound

Procedure

The reaction was carried out in analogy to reaction step 1.1 by reacting 2-(4-chloro-3-phenyl-1H-pyrazol-1-yl)nicotinic acid and 4-ethoxy-3-hydroxy-4-oxo-1-phenylbutan-2-aminium chloride. ESI-MS [M+H]+: 505.15

Workup

  1. customThe reaction was carried out in analogy to reaction step 1.1

Sources & evidence

ORD record
ord-6c1ef122a6aa4b74b91b23bf5f8d949a
Source dataset
uspto-grants-2015_06
Patent number
US09051304B2

Reaction notes

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