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3-Methoxy-2-(propan-2-yl)benzoyl chloride → HCID 22144559, compound

HRID 1824807
Notes
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Reaction equation

HRID 1824807 reaction equation
[Br:1][C:2]1[C:7]2[N:8]=C(C3C=CC(OC)=CC=3)[S:10][C:6]=2[CH:5]=[C:4]([O:19][CH3:20])[CH:3]=1.[CH:21]([C:24]1[C:32]([O:33][CH3:34])=[CH:31][CH:30]=[CH:29][C:25]=1[C:26](Cl)=O)([CH3:23])[CH3:22]>>[Br:1][C:2]1[C:7]2[N:8]=[C:26]([C:25]3[CH:29]=[CH:30][CH:31]=[C:32]([O:33][CH3:34])[C:24]=3[CH:21]([CH3:23])[CH3:22])[S:10][C:6]=2[CH:5]=[C:4]([O:19][CH3:20])[CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 221444983-Methoxy-2-(propan-2-yl)benzoyl chlorideHCID 22144553HCID 22144553, compound

Product 1

HCID 22144559HCID 22144559, compound

Procedure

The procedure was the same with 4-bromo-6-methoxy-2-(4-methoxy-phenyl)-benzothiazole except using 2-isopropyl-3-methoxy-benzoyl chloride instead of p-anisoyl chloride. Mass spec: MH+=392.

Sources & evidence

ORD record
ord-5fbc46bd2a3c450b9ac667c17a031a05
Source dataset
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07045539B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes