3-Formylphenylboronic acid → HCID 11199077, compound

HRID 2218031Notes

Reaction equation

HRID 2218031 reaction equation
Cl[C:2]1[C:3]2[CH:14]=[C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH:12]=[CH:11][C:4]=2[N:5]([CH3:10])[C:6](=[O:9])[CH2:7][N:8]=1.C(C1C=C(B(O)O)C=CC=1)=O.[CH3:32][O:33][C:34]1[CH:35]=[C:36](B(O)O)[CH:37]=[CH:38][CH:39]=1>>[CH3:32][O:33][C:34]1[CH:39]=[C:38]([C:2]2[C:3]3[CH:14]=[C:13]([C:15]4[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=4)[CH:12]=[CH:11][C:4]=3[N:5]([CH3:10])[C:6](=[O:9])[CH2:7][N:8]=2)[CH:37]=[CH:36][CH:35]=1

Participants

4

Reactant 3

HCID 27343563-Formylphenylboronic acidHCID 2734370(3-Methoxyphenyl)boronic acidHCID 69289305HCID 69289305, compound

Product 1

HCID 11199077HCID 11199077, compoundYield 10%

Procedure

Prepared from 5-Chloro-1-methyl-7-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-one using the same method described for Example 9 and instead of using 3-formylbenzene boronic acid, we used 3-methoxyphenyl boronic acid. The title compound (11 mg) was obtained as a yellow solid, (yield=10%).

Sources & evidence

ORD record
ord-e9b7af2aa15f499aae8ce5c23e26c7d1
Source dataset
uspto-grants-2008_08
Patent number
US07410963B2

Reaction notes

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