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HRID 1402735作成日:2026年10月25日

Dichloromethane → 1-Cyclobutyl-4-{[1-(piperidin-1-ylacetyl)azetidin-3-yl]carbonyl}-1,4-diazepane

https://huagongshe.com/reaction/1402735

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物PiperidineHCID 8082—
反応物1-{[1-(Chloroacetyl)azetidin-3-yl]carbonyl}-4-cyclobutyl-1,4-diazepaneHCID 66739334—
溶媒TolueneHCID 1140—
生成物Ammonia methanol dichloromethaneHCID 21584172—
生成物1-Cyclobutyl-4-{[1-(piperidin-1-ylacetyl)azetidin-3-yl]carbonyl}-1,4-diazepaneHCID 4685131953%

反応手順

A solution of 1-{[1-(chloroacetyl)azetidin-3-yl]carbonyl}-4-cyclobutyl-1,4-diazepane (40 mg, 0.13 mmol) and piperidine (38 μl, 0.38 mmol) in toluene (2 ml) was heated at 80° C. for 4 hrs in a sealed tube then cooled to RT. The reaction was diluted with DCM (30 ml), washed with a saturated aqueous solution of NaHCO3 (2×15 ml), dried (MgSO4), filtered and concentrated at reduced pressure. The residue was purified by silica FCC (using a gradient of eluents; DCM/MeOH/NH3 99:1:1 to 92:8:1) to give the title compound (25 mg, 53% yield) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08912176B2
出典データセットuspto-grants-2014_12
ORD IDord-d94c01dfbab6401088feab0f042d0515
出典メモuspto-grants-2014_12