4-Cyanobenzoyl chloride → HCID 68805840, compound

HRID 1715739Notes

Reaction equation

HRID 1715739 reaction equation
[CH:1]1([N:6]2[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]([NH:16][OH:17])=[NH:15])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[C:18]([C:20]1[CH:28]=[CH:27][C:23]([C:24]([Cl:26])=O)=[CH:22][CH:21]=1)#[N:19]>>[ClH:26].[CH:1]1([N:6]2[CH2:7][CH2:8][CH:9]([CH2:12][CH2:13][C:14]3[N:15]=[C:24]([C:23]4[CH:27]=[CH:28][C:20]([C:18]#[N:19])=[CH:21][CH:22]=4)[O:17][N:16]=3)[CH2:10][CH2:11]2)[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

3

Reactant 2

HCID 801724-Cyanobenzoyl chlorideHCID 178510925HCID 178510925, compound

Product 1

HCID 68805840HCID 68805840, compound

Procedure

The title compound was prepared by a similar procedure to that described in Example 1, starting from 3-(1-cyclopentylpiperidin-4-yl)-N-hydroxypropionamidine and 4-cyanobenzoyl chloride.

Sources & evidence

ORD record
ord-0243f203907645bc9c4a33485939b20c
Source dataset
uspto-grants-2010_09
Patent number
US07799924B2

Reaction notes

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