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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969353Generated: November 2, 2026

1,4-Bis(diphenylphosphino)butane → Ethyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylate

https://huagongshe.com/reaction/1969353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
ReactantSodium AcetateHCID 517045—
Reactant2,6-Dichloro-5-methoxypyrimidin-4-amineHCID 59126927—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
ProductEthyl 6-amino-2-chloro-5-methoxypyrimidine-4-carboxylateHCID 59126903232.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

2,6-Dichloro-5-methoxypyrimidin-4-ylamine (5.0 g, 26 mmol) was combined in 75 mL absolute ethanol with sodium acetate (2.1 g, 26 mmol), palladium acetate (280 mg, 0.91 mmol) and DPPB (1.1 g, 2.6 mmol) in a 300 mL stirred pressure reactor. The reactor was purged and pressurized to 300 psi with carbon monoxide, and heated at 110° C. for 7 h. The volatiles were removed under vacuum and the residue was taken up in ethyl acetate and water. The aqueous phase was extracted with an additional ethyl acetate; and the combined extracts were washed with brine, dried and evaporated. The residue was purified by flash chromatography on silica gel (0-30% ethyl acetate gradient in hexanes) to give the title compound (1.4 g, 23% yield): mp 118-119° C. 1H NMR (CDCl3) δ 6.18 (br s, 2H), 4.45 (q, 2H), 3.91 (s, 3H), 1.42 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426591B2
Source datasetuspto-grants-2013_04
ORD IDord-30c109e5066446bd97fb690ab9168687
Source noteuspto-grants-2013_04