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HRID 646628作成日:2026年10月26日

Cyanamide → 2-Chloro-5-[(methylsulfinyl)methyl]pyridine

https://huagongshe.com/reaction/646628

反応式

関与物質

役割名称HCID仕込み量
反応物CyanamideHCID 9864—
反応物2-Chloro-5-[(methylthio)methyl]pyridineHCID 20670360—
反応物2-[2-(Carboxylatomethyl)-3-iodophenyl]acetateHCID 21945688—
溶媒DichloromethaneHCID 6344—
生成物2-Chloro-5-[(methylsulfinyl)methyl]pyridineHCID 5926594518.6%

反応手順

To a solution of sulfide (A) (3.5 g, 17 mmol) and cyanamide (1.4 mg, 34 mmol) in CH2Cl2 (30 mL) at 0° C. was added iodobenzenediacetate (11.0 g, 34 mmol) all at once. The reaction was stirred for 30 min, then allowed to warm to room temperature overnight. The mixture was diluted with CH2Cl2 (50 mL) and washed with H2O. The aqueous layer was extracted with ethyl acetate (4×50 mL), and the combined organic layers were dried over MgSO4 and concentrated. The crude product was triturated with hexanes and purified by chromatography (chromatotron, 60% acetone/hexanes) to furnish the sulfilimine (B) as a yellow gum (0.60 g, 14%). IR (film) 3008, 2924, 2143, 1693 cm−1; 1H NMR (300 MHz, CDCl3) δ 8.8 (s, 1H), 8.0 (d, 1H), 7.8 (d, 1H), 4.5 (d, 1H), 4.3 (d, 1H), 2.9 (s, 3H); LC-MS (ESI): mass calcd for C9H9F3N3S [M+H]+ 248.04. Found 248.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705156B2
出典データセットuspto-grants-2010_04
ORD IDord-d238ff45d17146fa960fba9dfb7beb5c
出典メモuspto-grants-2010_04