2-Chlorobenzoyl chloride → HCID 11465553, compound

HRID 1593527Notes

Reaction equation

HRID 1593527 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:11][C:12]2[S:13][C:14]3[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:15]=3[N:16]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[Cl:24][C:25]1[CH:33]=[CH:32][CH:31]=[CH:30][C:26]=1[C:27](Cl)=[O:28]>>[Cl:24][C:25]1[CH:33]=[CH:32][CH:31]=[CH:30][C:26]=1[C:27]([N:11]([C:5]1[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=1)[C:12]1[S:13][C:14]2[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:15]=2[N:16]=1)=[O:28]

Participants

3

Reactant 2

HCID 691102-Chlorobenzoyl chlorideHCID 56553438HCID 56553438, compound

Product 1

HCID 11465553HCID 11465553, compound

Procedure

The title compound was synthesised from (3,4-Dimethoxy-phenyl)-(6-nitro-benzothiazol-2-yl)-amine and 2-chlorobenzoyl chloride (commercially available) according to the procedure described for Example 2. MS (m/e): 469.7 (MH+, 100%).

Sources & evidence

ORD record
ord-0f472012c0a040b48d1ea511adfa5954
Source dataset
uspto-grants-2007_11
Patent number
US07297707B2

Reaction notes

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