Phenylboronic Acid → HCID 16125935, compound

HRID 1267631Notes

Reaction equation

HRID 1267631 reaction equation
[C:1]1(B(O)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[C:11]1[CH:12]=[C:13]([CH:19]=[CH:20][N:21]=1)[C:14]([O:16][CH2:17][CH3:18])=[O:15]>>[C:1]1([C:11]2[CH:12]=[C:13]([CH:19]=[CH:20][N:21]=2)[C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 2762942Ethyl 2-chloroisonicotinate

Product 1

HCID 16125935HCID 16125935, compound

Procedure

Phenylboronic acid (147 mg) and ethyl 2-chloroisonicotinate (200 mg) were treated in the same manner as in Preparation Example 1 to obtain the title compound.

Sources & evidence

ORD record
ord-4b63646aebe946e48b3e6d7267dc88ff
Source dataset
uspto-grants-2003_04
Patent number
US06552188B2

Reaction notes

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