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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838078Generated: November 4, 2026

Water → HCID 18752900, compound

https://huagongshe.com/reaction/1838078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant3-Bromo-5-chloropyridin-2-amineHCID 2763971—
ReactantHCID 18752878HCID 18752878—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 18752900HCID 1875290040%

Reaction Steps

A solution of 3-bromo-5-chloro-2-pyridinamine (318 mg, 1.5 mmol), [(E)-2-(1,3-benzodioxol-5-yl)ethenyl](tributyl)stannane (250 mg, 1.7 mmol) (A. J. Bridges, A. Lee, C. E. Schwatrz, M. J. Towle, B. A. Littlefield, Bioorg. Med. Chem., 1993, 1, 403), palladium acetate (19 mg, 0.08 mmol) and tri-o-tolylphosphine (50 mg, 0.16 mmol) in DMF (0.5 ml) and triethylamine (0.5 ml) in a teflon pressure vessel was heated in a microwave (full power) for 20 sec, allowed to cool to RT heated in a microwave for a further 20 sec and then 1 min 20 sec. After allowing to cool, the reaction mixture was poured into water (20 ml) and extracted with EtOAc (3×20 ml). The combined extracts were washed with water (2×20 ml), dried over MgSO4 and concentrated. Recrystallisation from EtOAc—hexane gave the title compound as a brown solid (170 mg, 0.6 mmol):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673789B2
Source datasetuspto-grants-2004_01
ORD IDord-567c847ae5ef460297a6cd9d5c45f531
Source noteuspto-grants-2004_01