HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747855Generated: October 30, 2026
2-(Tributylstannyl)furan → HCID 178441006, compound
https://huagongshe.com/reaction/747855
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 67215339 | HCID 67215339 | — |
| Reactant | HCID 67215494 | HCID 67215494 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178441006 | HCID 178441006 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399761B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-986bd5ea2de24aec840d181961894982 |
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| Source note | uspto-grants-2008_07 |
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