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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407256생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/407256

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참여 물질

역할이름HCID투입량
반응물Methyl Tributylstannyl SulfideHCID 11110497—
반응물Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinateHCID 86668303—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Triphenylphosphine palladium dichlorideHCID 13169693—
생성물Methyl 4-amino-6-chloro-5-fluoro-3-(methylthio)picolinateHCID 86675417—

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온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6db71d26e3b54614ae953f66ae2e9360
출처 메모uspto-grants-2014_06