(3-Chlorophenyl)boronic acid → HCID 22337883, compound

Reaction equation

Br[C:2]1[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:25])([F:24])[F:23])(=[O:21])=[O:20])=[CH:13]3)=[CH:4][CH:3]=1.[Cl:28][C:29]1[CH:30]=[C:31](B(O)O)[CH:32]=[CH:33][CH:34]=1>>[Cl:28][C:29]1[CH:34]=[C:33]([C:2]2[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]3[CH:17]=[CH:16][CH:15]=[C:14]4[C:9]=3[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:24])([F:23])[F:25])(=[O:21])=[O:20])=[CH:13]4)=[CH:4][CH:3]=2)[CH:32]=[CH:31][CH:30]=1

Participants

Reactant 2

HCID 2734323(3-Chlorophenyl)boronic acid

HCID 22337880HCID 22337880, compound

Product 1

HCID 22337883HCID 22337883, compound

Procedure

The title compound was prepared from the product of Example 1 and 3-chlorophenyl boronic acid according to the procedure of Example 2, m.p. 170-171° C.

Sources & evidence

ORD record: ord-2f51222251a14aa291d96fe586b45a2b
Source dataset: uspto-grants-2005_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06933322B2

Reaction notes

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