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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-5-(tri-n-butylstannyl)imidazoleHCID 10915651—
ReactantHCID 90411776HCID 90411776—
SolventDimethylformamideHCID 6228—
ProductHCID 90411751HCID 90411751—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-33fa8d8599084a44b425a99e09700403
Source noteuspto-grants-2015_02