5-Chloro-2-methoxyphenylboronic acid → HCID 67240287, compound

HRID 1677884Notes

Reaction equation

HRID 1677884 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]2[CH:16]=[CH:15][C:14](Br)=[C:13]([CH3:18])[CH:12]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([O:29][CH3:30])=[C:24](B(O)O)[CH:25]=1>>[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([O:29][CH3:30])=[C:22]([C:14]2[CH:15]=[CH:16][C:11]([S:8]([C:5]3[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=3)(=[O:10])=[O:9])=[CH:12][C:13]=2[CH3:18])[CH:21]=1

Participants

3

Reactant 2

HCID 27357515-Chloro-2-methoxyphenylboronic acidHCID 68437422HCID 68437422, compound

Product 1

HCID 67240287HCID 67240287, compound

Procedure

The subtitle compound was prepared by the method of example 2 step (ii) using the product of step i) and 5-chloro-2-methoxybenzene boronic acid.

Sources & evidence

ORD record
ord-f97a93c35761421388f2964a029ff176
Source dataset
uspto-grants-2011_08
Patent number
US08008350B2

Reaction notes

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