1-Chloro-4-(4-isothiocyanatophenoxy)benzene → HCID 59464057, compound

HRID 1713783Notes

Reaction equation

HRID 1713783 reaction equation
[NH:1]([C:3](=[O:24])[C:4]([NH:6][C:7]1[CH:8]=[CH:9][C:10]([N:13]2[CH2:18][CH2:17][CH:16]([CH2:19][C:20]([O:22][CH3:23])=[O:21])[CH2:15][CH2:14]2)=[N:11][CH:12]=1)=[O:5])[NH2:2].[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([O:32][C:33]2[CH:38]=[CH:37][C:36]([N:39]=[C:40]=S)=[CH:35][CH:34]=2)=[CH:28][CH:27]=1>>[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([O:32][C:33]2[CH:38]=[CH:37][C:36]([NH:39][C:40]3[O:24][C:3]([C:4]([NH:6][C:7]4[CH:8]=[CH:9][C:10]([N:13]5[CH2:14][CH2:15][CH:16]([CH2:19][C:20]([O:22][CH3:23])=[O:21])[CH2:17][CH2:18]5)=[N:11][CH:12]=4)=[O:5])=[N:1][N:2]=3)=[CH:35][CH:34]=2)=[CH:28][CH:27]=1

Participants

3

Reactant 2

HCID 185373151-Chloro-4-(4-isothiocyanatophenoxy)benzeneHCID 59464312HCID 59464312, compound2×

Product 1

HCID 59464057HCID 59464057, compound

Procedure

Prepared using the procedures described above for Example 631 except using methyl [1-(5-{[hydrazino(oxo)acetyl]amino}pyridin-2-yl)piperidin-4-yl]acetate (Intermediate 77) and 1-chloro-4-(4-isothiocyanatophenoxy)benzene.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-091d6a49bc43458488b16a36281372f6
Source dataset
uspto-grants-2010_09
Patent number
US07795283B2

Reaction notes

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