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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645704Generated: October 25, 2026

Tetravinylstannane → 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/645704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetravinylstannaneHCID 66189—
Reactant2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 86628040—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 8662804129.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.45 g, 0.8 mmol) in dimethylformamide (2.0 mL) was added tetravinyltin (0.29 mL, 1.6 mmol) and tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) (0.092 g, 0.08 mmol). After degassing, the mixture was heated at 60° C. for 15 h. before it was diluted with EtOAc, and washed sequentially with Sat. NaHCO3 and brine. The organic extract was dried over Na2SO4 and concentrated to give a crude residue. Purification by flash column chromatography (Hexane/EtOAc=1:1) gave 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705004B2
Source datasetuspto-grants-2010_04
ORD IDord-f5ee33c6b49a4a03a14cc86261f53e97
Source noteuspto-grants-2010_04