戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 540017作成日:2026年10月26日

3-(Aminomethyl)oxetan-3-amine → [4-{[(3-Aminooxetan-3-yl)methyl]amino}-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinolin-6-yl]methanol

https://huagongshe.com/reaction/540017

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Aminomethyl)oxetan-3-amineHCID 21713016—
反応物4-Chloro-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-quinoline-6-methanolHCID 71254465—
生成物[4-{[(3-Aminooxetan-3-yl)methyl]amino}-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinolin-6-yl]methanolHCID 71262090—

反応手順

The title compound was prepared in analogy to Example 3-1 in Scheme 5 by using 4-chloro-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)-quinoline-6-methanol and 3-(aminomethyl)oxetan-3-amine. MS obsd. (ESI+) [(M+H)+] 455, 1H NMR (400 MHz, CD3OD) δ ppm 8.33 (s, 1 H), 8.08-8.05 (d, J=11.2 Hz, 2 H), 7.94-7.92 (d, J=7.2 Hz, 1 H), 7.74-7.68 (m, 3 H), 7.57-7.53 (t, J=7.6 Hz, 1 H), 6.26 (s, 1 H), 5.31 (s, 2 H), 4.72 (s, 2 H), 44.57 (s, 4 H), 4.44 (s, 1 H), 3.88 (s, 2 H), 3.77-3.71 (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-c0b3c89d2ccf4dfbaa066dbcc259e185
出典メモuspto-grants-2014_10