4-Chlorophenylboronic acid → HCID 59809604, compound

HRID 2354338Notes

Reaction equation

HRID 2354338 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](B(O)O)=[CH:4][CH:3]=1.Br[C:12]1[CH:13]=[C:14]([CH:18]([N:25]([CH3:39])[C:26](=[O:38])[CH2:27][N:28]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=2)[CH3:29])[CH2:19][N:20]2[CH2:24][CH2:23][CH2:22][CH2:21]2)[CH:15]=[CH:16][CH:17]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH:18]([N:25]([CH3:39])[C:26](=[O:38])[CH2:27][N:28]([C:30]3[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=3)[CH3:29])[CH2:19][N:20]3[CH2:24][CH2:23][CH2:22][CH2:21]3)[CH:13]=2)=[CH:4][CH:3]=1

Participants

3

Procedure

The title compound was prepared according to the procedure described for example 33, using 4-chlorophenylboronic acid and the intermediate from step c) above. MS (ES) m/e 532 [M+H]+.

Sources & evidence

ORD record
ord-b09638e98971441f92d7ea9a958c8155
Source dataset
uspto-grants-2010_07
Patent number
US07749998B2

Reaction notes

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