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HRID 9106作成日:2026年10月26日

Diethyl Ether → 1-(7-Oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea

https://huagongshe.com/reaction/9106

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Ethyl isocyanateHCID 8022—
反応物TriethylamineHCID 8471—
反応物2-Amino-4,5,6,7-tetrahydro-1,3-benzothiazol-7-oneHCID 587850—
溶媒DimethylformamideHCID 6228—
生成物1-(7-Oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-ureaHCID 2198555785%

反応条件

温度90 °C

反応手順

A solution of 2-amino-7-oxo-4,5,6,7-tetrahydro-benzothiazole 3 (11.56 g, 68.7 mmol) in anhydrous DMF (200 mL) was treated with triethylamine (19.2 mL, 137 mmol, 2.0 eq) and ethyl isocyanate (10.9 nL, 137 mmol, 2.0 eq). The reaction mixture was heated at about 90° C. with stirring for about 3 hours. The DMF solvent was distilled off under reduced pressure. A sticky brown residue was obtained. Treatment with Et2O (100 mL) gave a precipitate, which was filtered off and washed with more Et2O (50 mL). The light brown colored solid was dried under vacuum to give 13.97 g (85%) of 4. The material was used in the following synthesis without further purification. 1H NMR (DMSO) δ 10.95 (br s, 1H, NH), 6.66 (br s, 1H, NH), 3.16 (p, 2H, J=7.2 Hz, CH2), 2.79 (t, 2H, J=6.1 Hz, CH2), 2.45 (t, 2H, J=6.5 Hz, CH2), 2.05 (p, 2H, J=6.4 Hz, CH2), 1.07 (t, 3H, J=7.2 Hz, CH3); LC/MS 240 (MH+); RP-HPLC RT 2.27 minutes.

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-0f07a300f177487084962573f64fed09
出典メモuspto-grants-2006_08