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1033772-29-0

5-FORMYL-1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER synthesis

1synthesis methods
201230-82-2 Synthesis
carbon monoxide

201230-82-2
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78155-74-5 Synthesis
METHYL 5-BROMO-1H-INDAZOLE-3-CARBOXYLATE

78155-74-5
115 suppliers
$9.00/100mg

5-FORMYL-1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER

1033772-29-0
14 suppliers
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Yield:1033772-29-0 54%

Reaction Conditions:

bis-triphenylphosphine-palladium(II) chloride in N,N-dimethyl-formamide at 110; for 6 h;

Steps:

3.A

A: A mixture of 5-bromo-1 H-indazole-3-carboxylic acid methyl ester (1 g, 3.92 mmol), HCOONa (400 mg, 5.88 mmol), and PdCI2(PPh3)2 (138 mg, 0.2 mmol) in DMF (10 mL) was put under vacuum, and charged with CO. This process was repeated three times, and the mixture was kept at 110 0C for 6 hr. The reaction mixture was cooled to rt, diluted with EtOAc and water, and extracted. The organic phase was dried and concentrated. Purification via flash chromatography afforded 5-formyl-1H-indazole-3-carboxylic acid methyl ester (430 mg, 54%).

References:

WO2008/71451,2008,A1 Location in patent:Page/Page column 58

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