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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663009Generated: October 28, 2026

2-(Tributylstannyl)furan → HCID 67215494, compound

https://huagongshe.com/reaction/1663009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 67215339HCID 67215339—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductHCID 67215494HCID 67215494—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 366 mg (0.76 mMol) 1-(4-tert-butyl-anilino)-4-[5-bromo-6-methoxy-(pyridin-3-yl)-methyl]phthalazine (Ex. 17: a) in 7 ml degassed DMF under a N2-atmosphere are added 174 mg (0.15 mMol) of Pd[P(C6H5)3]4 and 0.6 ml (1.9 mMol) of 2-tributylstannyl-furan (Aldrich). After 4 h stirring at 100° C., the reaction mixture is diluted with EtOAc and washed with NaHCO3 solution. The aqueous layers are extracted twice with EtOAc, the organic phases washed with water, brine, dried (Na2SO4) and concentrated in vacuo. Column chromatography (SiO2; CH2Cl2/Et2O 7:3) and crystallization from DIPE yields the title compound. mp: 180-182° C.; ES-MS: (M+H)+=465; HPLC(Grad20-100) tRet=15.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034814B2
Source datasetuspto-grants-2011_10
ORD IDord-3b083db176c84484ba7b8f8447e33c33
Source noteuspto-grants-2011_10