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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 646628Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/646628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanamideHCID 9864—
Edukt2-Chloro-5-[(methylthio)methyl]pyridineHCID 20670360—
Edukt2-[2-(Carboxylatomethyl)-3-iodophenyl]acetateHCID 21945688—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Chloro-5-[(methylsulfinyl)methyl]pyridineHCID 5926594518,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705156B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-d238ff45d17146fa960fba9dfb7beb5c
Quellennotizuspto-grants-2010_04