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HRID 407256作成日:2026年10月26日

Methyl Tributylstannyl Sulfide → Methyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinate

https://huagongshe.com/reaction/407256

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl Tributylstannyl SulfideHCID 11110497—
反応物Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinateHCID 86668303—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Triphenylphosphine palladium dichlorideHCID 13169693—
生成物Methyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinateHCID 86675417—

反応条件

温度80 °C

反応手順

Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinate (1.5 g, 4.6 mmol), tri-n-butylmethylthiostannane (2.5 g, 7.3 mmol), his (triphenylphosphine) palladium (II) chloride (320 mg, 0.46 mmol) and copper (I) iodide (90 mg, 0.46 mmol) were combined 15 ml dry, deaerated DMF and heated to 80° C. After 3 h another 2.5 g portion of the stannane were added and heating was continued for 18 h. After cooling, the mixture was stirred with 25 ml 10% potassium bifluoride solution for 20 ml. The heterogeneous mixture was stirred with 100 ml ethyl acetate and filtered through diatomaceous earth to remove curdy solids. The separated organic phase was washed twice with 15 ml water, 15 ml sat. NaCl, dried (Na2SO3) and evaporated. The product was purified by silica gel chromatography eluting with a 0-25% ethyl acetate-DCM gradient. The gummy residue was stirred with hexane to produce the written product as a white solid, 800 mg. Mp: 75-77° C. 1H NMR (400 MHz, CDCl3) δ 5.35 (s, 2H), 3.96 (s, 3H), 2.33 (s, 3H). 19F NMR (376 MHz, CDCl3) δ −138.81. EIMS m/z 250.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754229B2
出典データセットuspto-grants-2014_06
ORD IDord-6db71d26e3b54614ae953f66ae2e9360
出典メモuspto-grants-2014_06