5-Chloro-2-methoxyphenylboronic acid → HCID 67238967, compound

HRID 1677874Notes

Reaction equation

HRID 1677874 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)=[CH:13][CH:12]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[Cl:18][C:19]1[CH:20]=[CH:21][C:22]([O:28][CH3:29])=[C:23](B(O)O)[CH:24]=1>>[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([O:28][CH3:29])=[C:21]([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][CH:13]=2)[CH:20]=1

Participants

3

Reactant 2

HCID 27357515-Chloro-2-methoxyphenylboronic acidHCID 14711968HCID 14711968, compound

Product 1

HCID 67238967HCID 67238967, 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-1ec5557d734340419a9bfc022e7b5f0e
Source dataset
uspto-grants-2011_08
Patent number
US08008350B2

Reaction notes

Loading…