HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510054Generated: October 25, 2026
Ethyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylate → HCID 66614187, compound
https://huagongshe.com/reaction/510054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylate | HCID 4390083 | — |
| Reactant | Hexabutyldistannane | HCID 6327815 | — |
| Reactant | 5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridine | HCID 58065602 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66614187 | HCID 66614187 | — |
Reaction Steps
Under argon, 3.85 g (10.91 mmol) of the compound from example 24A were initially charged in dioxane (100 ml) and the reaction mixture was purged with argon. Subsequently, 8.27 ml (16.36 mmol) of hexabutylditin and 2.96 g (12.00 mmol) of ethyl 6-amino-2-chloro-5-nitropyrimidine-4-carboxylate (prepared according to J. Chem. Res. 1989, 2086-2097) were added. Thereafter, 3.83 g (5.45 mmol) of bis(triphenylphosphine)palladium(II) chloride were added and the reaction mixture was stirred at 100° C. overnight. Thereafter, the mixture was cooled to RT and filtered through Celite, and the residue was washed with methanol. The filtrate was concentrated, and the residue was extracted by stirring with ethyl acetate and filtered off. The filtrate was concentrated and the residue was purified by means of prep. HPLC (eluent: acetonitrile/water with 0.1% formic acid gradient). This gave 1.36 g (71% purity, 14% of theory) of crude product, which was converted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096592B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-60ec768fa4434d84970c61afd5162e51 |
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| Source note | uspto-grants-2015_08 |
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