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HRID 1484431作成日:2026年10月27日

Methyl p-toluenesulfonate → N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester

https://huagongshe.com/reaction/1484431

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl p-toluenesulfonateHCID 6645—
反応物2,3-Diazaspiro[4.4]non-3-ene-2-carbothioic acid ethylamideHCID 53354135—
溶媒MethanolHCID 887—
生成物N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 5335423131.9%

反応手順

To a solution of 1.0 g (4.7 mmol) 2,3-diazaspiro[4.4]non-3-ene-2-carbothioic acid ethylamide in 10 mL methanol was added 1.1 g (5.7 mmol) methyl p-toluenesulfonate. The mixture was refluxed for 48 hrs and concentrated under reduced pressure. The residue was triturated with 30 mL diethyl ether and all volatiles were removed from the isolated oily product under reduced pressure. The residual oil was taken up in 40 mL dichloromethane and extracted 3 times with a saturated aqueous NaHCO3 solution. The organic layer was dried over MgSO4, filtered and evaporated to dryness under reduced pressure to afford 0.33 g (1.5 mmol, 31%) of N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester as a light-brown oil. 1H NMR identical to spectrum obtained from material prepared by using iodomethane as methylating agent (vide supra).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09422244B2
出典データセットuspto-grants-2016_08
ORD IDord-6209b586cd7b410b84c80f7fb694d0a0
出典メモuspto-grants-2016_08