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HRID 244069作成日:2026年10月26日

Diisopropylethylamine → Methyl 1-{[(3-chloro-2'-{4-chloro-3-[3-(dimethylamino)propoxy]-phenyl}-5-methyl-2,3'-bipyridin-6'-yl)carbonyl]amino}cyclohexane-carboxylate hydrochloride

https://huagongshe.com/reaction/244069

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物Methyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
反応物3-Chloro-2'-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-5-methyl-2,3'-bipyridine-6'-carboxylic acidHCID 66840942—
溶媒AcetonitrileHCID 6342—
生成物Methyl 1-{[(3-chloro-2'-{4-chloro-3-[3-(dimethylamino)propoxy]-phenyl}-5-methyl-2,3'-bipyridin-6'-yl)carbonyl]amino}cyclohexane-carboxylate hydrochlorideHCID 66840590—

反応条件

温度0 °C

反応手順

To a suspension of 134 mg (0.29 mmol) of 3-chloro-2′-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-5-methyl-2,3′-bipyridine-6′-carboxylic acid in 5 mL of anhydrous acetonitrile are successively added 0.18 mL (1.02 mmol) of DIEA and 56 mg (0.29 mmol) of methyl 1-aminocyclohexanecarboxylate hydrochloride. The mixture is cooled to 0° C. and 112 mg (0.35 mmol) of TBTU are added. After stirring for 18 hours between 0 and 10° C., the reaction medium is concentrated under reduced pressure and then taken up in 20 mL of a 1/1 EtOAc/ether mixture. After washing with 10 mL of water and 10 mL of saturated aqueous NaHCO3 solution, the organic phase is dried over Na2SO4 and concentrated under reduced pressure. 0.2 mL (0.1 mmol) of a 2N solution of HCl in ether and then 20 mL of anhydrous ether are added to the residue, taken up in 5 mL of DCM, which allows precipitation of 139 mg of methyl 1-{[(3-chloro-2′-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-5-methyl-2,3′-bipyridin-6′-yl)-carbonyl]amino}cyclohexanecarboxylate hydrochloride in the form of a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653276B2
出典データセットuspto-grants-2014_02
ORD IDord-82e6e57a8dcb47a1aa1e5a73e29b4e15
出典メモuspto-grants-2014_02