2,5-Dichlorobenzeneboronic acid → HCID 86679885, compound

HRID 1519395Notes

Reaction equation

HRID 1519395 reaction equation
C[O:2][C:3](=[O:24])[C:4]1[CH:9]=[C:8]([C:10]2[S:11][CH:12]=[C:13]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=3)[N:14]=2)[CH:7]=[CH:6][C:5]=1Br.[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:27]=1B(O)O>>[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:27]=1[C:5]1[C:4]([C:3]([OH:2])=[O:24])=[CH:9][C:8]([C:10]2[S:11][CH:12]=[C:13]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([Cl:22])[CH:16]=3)[N:14]=2)=[CH:7][CH:6]=1

Participants

3

Reactant 2

HCID 27733712,5-Dichlorobenzeneboronic acidHCID 86679833Methyl 2-bromo-5-(4-(3,4-dichlorophenyl)thiazol-2-yl)benzoate2×

Product 1

HCID 86679885HCID 86679885, compoundYield 32.3%

Procedure

Using the conditions of General Procedure B for Suzuki Coupling and Hydrolysis in Parallel Mode, 2-bromo-5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-benzoic acid methyl ester (which may be prepared as described for Intermediate 6; 89 mg, 0.2 mmol) was reacted with 2,5-dichlorophenylboronic acid (available from Combi-Blocks Inc.; 76 mg, 0.4 mmol). The resulting ester was hydrolyzed and the acid was purified to give 2′,5′-dichloro-4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-biphenyl-2-carboxylic acid (32 mg, 32%). 1H NMR (400 MHz, DMSO-d6) δ 13.18 (br s, 1H), 8.56 (s, 1H), 8.50 (s, 1H), 8.34 (s, 1H), 8.29 (d, J=8.0 Hz, 1H), 8.10 (d, J=8.5 Hz, 1H), 7.77 (d, J=7.3 Hz, 1H), 7.54-7.57 (m, 1H), 7.49 (s, 1H), 7.47 (s, 2H).

Workup

  1. customthe acid was purified

Sources & evidence

ORD record
ord-9b3c84f09b8f4b0d82f90f41f6c772dc
Source dataset
uspto-grants-2015_07
Patent number
US09073881B2

Reaction notes

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