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HRID 233704作成日:2026年10月26日

2-Amino-4,5,6,7-tetrahydrobenzothiazole → N-[2-(1-cyclohexenyl)ethyl]-N'-[4,5,6,7-tetrahydrobenzothiazolyl]thiourea

https://huagongshe.com/reaction/233704

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4,5,6,7-tetrahydrobenzothiazoleHCID 18046—
反応物1-(2-Isothiocyanatoethyl)cyclohex-1-eneHCID 2735881—
溶媒DimethylformamideHCID 6228—
生成物N-[2-(1-cyclohexenyl)ethyl]-N'-[4,5,6,7-tetrahydrobenzothiazolyl]thioureaHCID 1970390113.3%

反応手順

A solution of 2-(1-cyclohexenyl)ethyl isothiocyanate (1.67 g, 10 mmol) and 2-amino-4,5,6,7-tetrahydrobenzothiazole (1.54 g, 10 mmol) in N,N-dimethylformamide (100 mL) was heated at 100° C. for 120 h. The reaction was cooled to room temperature, the solvent removed under reduced pressure, the residue taken up in ethyl acetate and washed with 1N HCl. The organic layer was concentrated and the residue recrystallized from ethyl acetate-hexanes to provide 426 mg (13%) of the titled product:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593993
出典データセットuspto-grants-1997_01
ORD IDord-d5c227c25b4b45b1b6cd865fee535c41
出典メモuspto-grants-1997_01