4-Acetylphenylboronic acid → HCID 11272375, compound

HRID 1455655Notes

Reaction equation

HRID 1455655 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([C:14]2[CH:15]=[C:16]([C:24]([CH3:30])([S:26]([CH3:29])(=[O:28])=[O:27])[CH3:25])[CH:17]=[C:18]3[C:23]=2[N:22]=[CH:21][CH:20]=[CH:19]3)[CH:9]=1.[C:31]([C:34]1[CH:39]=[CH:38][C:37](B(O)O)=[CH:36][CH:35]=1)(=[O:33])[CH3:32]>CCOC(C)=O>[CH3:30][C:24]([C:16]1[CH:17]=[C:18]2[C:23](=[C:14]([C:10]3[CH:9]=[C:8]([C:3]4[C:2]([C:37]5[CH:38]=[CH:39][C:34]([C:31](=[O:33])[CH3:32])=[CH:35][CH:36]=5)=[CH:7][CH:6]=[CH:5][CH:4]=4)[CH:13]=[CH:12][CH:11]=3)[CH:15]=1)[N:22]=[CH:21][CH:20]=[CH:19]2)([S:26]([CH3:29])(=[O:28])=[O:27])[CH3:25]

Participants

4

Procedure

Prepared according to the general procedure Coupling-1 using bromide from step 1 and 4-acetylbenzeneboronic acid as starting material. Flash chromatography (Hex:EtOAc; 50:50) afforded the title compound.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-36cbc24258064d7991fdeed32a9be628
Source dataset
uspto-grants-2009_01
Patent number
US07482456B2

Reaction notes

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