4-Acetylbenzoyl chloride → HCID 68814112, compound

HRID 2055706Notes

Reaction equation

HRID 2055706 reaction equation
[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]([NH:12][OH:13])=[NH:11])[CH2:6][CH2:5]1)([CH3:3])[CH3:2].[C:14]([C:17]1[CH:25]=[CH:24][C:20]([C:21]([Cl:23])=O)=[CH:19][CH:18]=1)(=[O:16])[CH3:15]>>[ClH:23].[CH:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[N:11]=[C:21]([C:20]3[CH:24]=[CH:25][C:17]([C:14](=[O:16])[CH3:15])=[CH:18][CH:19]=3)[O:13][N:12]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 134096034-Acetylbenzoyl chlorideHCID 178456252HCID 178456252, compound

Product 1

HCID 68814112HCID 68814112, compound

Procedure

The title compound was prepared by a similar procedure to that described in Example 56, starting from 1-isopropyl-N-hydroxypiperidine-4-carboxamidine and 4-acetylbenzoyl chloride.

Sources & evidence

ORD record
ord-debb4b268cb34787a316a3a259ef6c66
Source dataset
uspto-grants-2008_02
Patent number
US07332508B2

Reaction notes

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