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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747855Generated: October 30, 2026

2-(Tributylstannyl)furan → HCID 178441006, compound

https://huagongshe.com/reaction/747855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantHCID 67215339HCID 67215339—
ReactantHCID 67215494HCID 67215494—
SolventEthyl AcetateHCID 8857—
ProductHCID 178441006HCID 178441006—

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(4-tert-Butyl-anilino)4[5-(furan-2-yl)-6-methoxy-(pyridin-3-yl)-methyl]phthalazine: 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-atmoshere are added 174 mg (0.15 mMol) of Pd[P(C8H5)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 vacuuo. Column chromatography (SiO2; CH2Cl2/Et2O 7:3) and cristalization 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 numberUS07399761B2
Source datasetuspto-grants-2008_07
ORD IDord-986bd5ea2de24aec840d181961894982
Source noteuspto-grants-2008_07