Phenylboronic Acid → HCID 67343442, compound

HRID 1850086Notes

Reaction equation

[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([O:12][C:13]2[CH:18]=[C:17](Br)[C:16]([CH3:20])=[CH:15][C:14]=2[C:21]#[N:22])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[C:23]1(B(O)O)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([O:12][C:13]2[CH:18]=[C:17]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:16]([CH3:20])=[CH:15][C:14]=2[C:21]#[N:22])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

Reactant 2

HCID 66827Phenylboronic Acid

HCID 67343910HCID 67343910, compound

Product 1

HCID 67343442HCID 67343442, compound

Procedure

Prepared from the title compound of Step A as described in Example 1 Step E using phenylboronic acid.

Sources & evidence

ORD record: ord-e3ec162e57d647cbbba7f5f41c783cdb
Source dataset: uspto-grants-2015_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08957059B2

Reaction notes

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