4-(Methanesulfonyl)benzoyl chloride → HCID 68804590, compound

HRID 2055673Notes

Reaction equation

HRID 2055673 reaction equation
[CH:1]1([N:6]2[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][CH2:14][C:15]([NH:17][OH:18])=[NH:16])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:19][S:20]([C:23]1[CH:31]=[CH:30][C:26]([C:27]([Cl:29])=O)=[CH:25][CH:24]=1)(=[O:22])=[O:21]>>[ClH:29].[CH:1]1([N:6]2[CH2:7][CH2:8][CH:9]([CH2:12][CH2:13][CH2:14][C:15]3[N:16]=[C:27]([C:26]4[CH:25]=[CH:24][C:23]([S:20]([CH3:19])(=[O:22])=[O:21])=[CH:31][CH:30]=4)[O:18][N:17]=3)[CH2:10][CH2:11]2)[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

3

Reactant 2

HCID 112760134-(Methanesulfonyl)benzoyl chlorideHCID 178510956HCID 178510956, compound

Product 1

HCID 68804590HCID 68804590, compound

Procedure

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

Sources & evidence

ORD record
ord-5bd350e6b2d346f9870430d3d81c3eb6
Source dataset
uspto-grants-2008_02
Patent number
US07332508B2

Reaction notes

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