Phenylboronic Acid → HCID 18512285, compound

HRID 1370822Notes

Reaction equation

[F:1][C:2]1[CH:28]=[C:27]([F:29])[CH:26]=[CH:25][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][C:18]=1[F:24])[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15].[C:30]1(B(O)O)[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[F:1][C:2]1[CH:28]=[C:27]([F:29])[CH:26]=[CH:25][C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[CH:19][C:18]=1[F:24])[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[C:7]=1[CH3:15]

Participants

Reactant 2

HCID 66827Phenylboronic Acid

HCID 18511989HCID 18511989, compound

Product 1

HCID 18512285HCID 18512285, compound

Procedure

The product from Example 53E and phenylboronic acid were processed as described in Example 48A to provide the title compound.

Sources & evidence

ORD record: ord-8df6417d7828450b98adb2c3438aab66
Source dataset: uspto-grants-2003_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06583180B2

Reaction notes

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