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HRID 540175作成日:2026年10月25日

1,3-dihydro-1,3-dioxo-2H-isoindole-2-propionyl chloride → N-[2-(1,1-Dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-6-methylquinolin-4-yl]-beta-alaninamide

https://huagongshe.com/reaction/540175

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-dihydro-1,3-dioxo-2H-isoindole-2-propionyl chlorideHCID 86966—
反応物3-Amino-N-[2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-6-methylquinolin-4-yl]-4,4,4-trifluorobutanamideHCID 71255425—
反応物HCID 71255483HCID 71255483—
生成物N-[2-(1,1-Dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-6-methylquinolin-4-yl]-beta-alaninamideHCID 71262130—

反応手順

The title compound was prepared in analogy to 3-amino-N-[2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-6-methylquinolin-4-yl]-4,4,4-trifluorobutanamide in Example 42-1 in Scheme 19 by using 2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-6-methylquinolin-4-amine and 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propanoyl chloride. MS obsd. (ESI+) [(M+H)+] 425, 1H NMR (400 MHz, CDCl3) δ ppm 8.00 (d, J=7.83 Hz, 1 H), 8.29 (s, 1 H), 7.85 (d, J=7.33 Hz, 1 H), 7.61-7.47 (m, 4 H), 7.34 (d, J=12.13 Hz, 2 H), 5.12 (s, 2 H), 3.55 (brs, 2 H), 3.23 (d, J=5.56 Hz, 2 H), 2.62 (brs, 2 H), 2.44 (brs, 3 H), 1.66-2.10 (m, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871756B2
出典データセットuspto-grants-2014_10
ORD IDord-c5b5151fb93f4dbc8a4c088659878412
出典メモuspto-grants-2014_10