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HRID 9155作成日:2026年10月26日

Formaldehyde → 2-(3-Ethyl-5-methyl-2-oxo-1,3,5-triazinan-1-yl)-4,5,6,7-tetrahydro-1,3-benzothiazol-7-one

https://huagongshe.com/reaction/9155

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物MethylamineHCID 6329—
反応物4-MethylmorpholineHCID 7972—
反応物1-(7-Oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-ureaHCID 21985557—
溶媒Water ethanolHCID 19096565—
生成物2-(3-Ethyl-5-methyl-2-oxo-1,3,5-triazinan-1-yl)-4,5,6,7-tetrahydro-1,3-benzothiazol-7-oneHCID 69652434100.9%

反応条件

温度60 °C

反応手順

To a suspension of N-ethyl-N′-(7-oxo-4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)urea (10.0 g, 41.79 mmol) in EtOH/H2O (1/1, 300 mL) were added formaldehyde (37 wt % in H2O, 20.4 g, 417.87 mmol), methylamine (40 wt % in H2O, 10.8 mL, 125.37 mmol) and N-methylmorpholine (11.8 mL, 83.6 mmol). The suspension was heated to about 60° C. for about 5 hrs, then a solution had been formed. The reaction mixture was pumped down in vacuo to give 12.41 g (quantitative yield) pure product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091227B2
出典データセットuspto-grants-2006_08
ORD IDord-18fdaa5a2062445dbc2788aa4294d857
出典メモuspto-grants-2006_08