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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370592Generated: October 29, 2026

Water → HCID 18752900, compound

https://huagongshe.com/reaction/1370592

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 numberUS06583162B1
Source datasetuspto-grants-2003_06
ORD IDord-8af0a66f73f94494bb11ee15c44d86ed
Source noteuspto-grants-2003_06