2-Acetoxyisobutyroyl chloride → HCID 16045475, compound

HRID 1393259Notes

Reaction equation

HRID 1393259 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:19]3[CH2:20][CH2:21][CH2:22][CH:12]2[C:13]2[CH:14]=[N:15][NH:16][C:17]=2[CH2:18]3)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[C:23]([O:26][C:27]([CH3:32])([CH3:31])[C:28](Cl)=[O:29])(=[O:25])[CH3:24]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:19]3[CH2:20][CH2:21][CH2:22][CH:12]2[C:13]2[C:17]([CH2:18]3)=[N:16][N:15]([C:28](=[O:29])[C:27]([O:26][C:23](=[O:25])[CH3:24])([CH3:32])[CH3:31])[CH:14]=2)(=[O:9])=[O:10])=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 1234962-Acetoxyisobutyroyl chlorideHCID 16045311HCID 16045311, compound

Product 1

HCID 16045475HCID 16045475, compound

Procedure

Prepared by acylation of 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-diene using 2-acetoxyisobutyryl chloride.

Sources & evidence

ORD record
ord-1d06da3d4d9f41f9a3c16b45ab9d7aa7
Source dataset
uspto-grants-2008_03
Patent number
US07345056B2

Reaction notes

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