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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927196Generated: October 25, 2026

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

https://huagongshe.com/reaction/1927196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
Reactant2-Chloro-5-[(methylthio)methyl]pyridineHCID 20670360—
Reactant2-[2-(Carboxylatomethyl)-3-iodophenyl]acetateHCID 21945688—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-[(methylsulfinyl)methyl]pyridineHCID 5926594518.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183268B2
Source datasetuspto-grants-2012_05
ORD IDord-f10bb45e1fde44d0a11e63cefeb6805c
Source noteuspto-grants-2012_05