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HRID 1161645作成日:2026年10月26日

Diisopropylethylamine → (+/-) N-(3-{[2-(12,12-Dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-N-methyl-methanesulfonamide

https://huagongshe.com/reaction/1161645

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物N-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamideHCID 45480403—
反応物(+/-) (4-Chloro-5-trifluoromethyl-pyrimidin-2-yl)-(12,12-dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-yl)-amineHCID 86761198—
溶媒Dichloroethane t-butanolHCID 86704321—
生成物(+/-) N-(3-{[2-(12,12-Dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-N-methyl-methanesulfonamideHCID 5951890818%

反応条件

温度85 °C

反応手順

A mixture of C6 (51 mg; 0.126 mmol) and 1:1 (vol:vol) t-BuOH/dichloroethane (500 μL) was added to a mixture of N-(3-Aminomethyl-pyridin-2-yl)-N-methyl-methanesulfonamide (38 mg, 0.139 mmol) and diisopropyl ethylamine (66 μL, 0.378 mmol). The reaction mixture was heated to 85° C. in a sealed vial. After two hours, the hot reaction mixture was loaded directly onto silica under reduced pressure, purified via chromatography (99:1:0.1 CHCl3:CH3OH:NH4OH), and concentrated under reduced pressure to provide 1 as a white solid (13 mg, 0.0223 mmol, 18%). LC/MS (Method F) r.t.=2.26 min.; m/z 583.2. HPLC r.t.=6.40 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07820648B2
出典データセットuspto-grants-2010_10
ORD IDord-98a7861602504b46a4637384b2933871
出典メモuspto-grants-2010_10