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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Bromo-1,7-dimethyl-1H-indazole | HCID 37819125 | — |
| Reactant | 6-Chloro-pyrimidine-4-carboxylic acidmethoxy-methyl-amide | HCID 58181216 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-chloro-pyrimidin-4-yl)-(1,7-dimethyl-1H-indazol-5-yl)-methanone | HCID 58181127 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629137B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-c497278f1e9545689718fc3bd337f193 |
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| Source note | uspto-grants-2014_01 |
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