HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850702Generated: October 30, 2026
1-Methyl-5-(tri-n-butylstannyl)imidazole → HCID 90411751, compound
https://huagongshe.com/reaction/1850702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methyl-5-(tri-n-butylstannyl)imidazole | HCID 10915651 | — |
| Reactant | HCID 90411776 | HCID 90411776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 90411751 | HCID 90411751 | — |
Reaction Steps
2-amino-N-(4-bromo-3-methyl-isothiazol-5-yl)-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxamide (20 mg, 0.05388 mmol), tributyl-(3-methylimidazol-4-yl)stannane (40.01 mg, 0.1078 mmol) dichloropalladium triphenylphosphane (7.566 mg, 0.01078 mmol) in DMF (2 mL) was degassed for 5 min, then heated at 110° C. After 2 h, the reaction mixture was loaded on a SCX column, washed with DCM/MeOH mixtures. The product was eluted with a 2M solution of ammonia in MeOH and the eluent was concentrated in vacuo. The residue was purified by fractionlynx to yield 2-amino-6-fluoro-N-(3-methyl-4-(1-methyl-1H-imidazol-5-yl)isothiazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide as a pale yellow solid. (8.09 mg, 37.4%). MS (ES+) 373.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957078B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-33fa8d8599084a44b425a99e09700403 |
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| Source note | uspto-grants-2015_02 |
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