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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469362Generated: October 30, 2026

Sodium Bicarbonate → (6-chloro-pyrimidin-4-yl)-(1,7-dimethyl-1H-indazol-5-yl)-methanone

https://huagongshe.com/reaction/469362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-1,7-dimethyl-1H-indazoleHCID 37819125—
Reactant6-Chloro-pyrimidine-4-carboxylic acidmethoxy-methyl-amideHCID 58181216—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(6-chloro-pyrimidin-4-yl)-(1,7-dimethyl-1H-indazol-5-yl)-methanoneHCID 58181127—

Reaction Conditions

Temperature-75 °C

Reaction Steps

Under an argon atmosphere 0.450 g (2.00 mmol) 5-bromo-1,7-dimethyl-1H-indazole in 25 mL THF were cooled to −75° C., combined with 1.40 mL (2.24 mmol) of a 1.6 molar n-butyllithium solution and stirred for 1 h at −75° C. Then 0.480 g (2.14 mmol) 6-chloro-pyrimidine-4-carboxylic acid methoxy-methyl-amide were added dropwise. The mixture was brought to 0° C. and stirred for a further hour. Then saturated sodium hydrogen carbonate solution was stirred in, the mixture was extracted with EtOAc, the organic phase was dried and evaporated down i. vac. The residue was triturated with DIPE, suction filtered and dried. The precipitate was purified by flash chromatography (Alox).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-c497278f1e9545689718fc3bd337f193
Source noteuspto-grants-2014_01