戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 33299作成日:2026年10月23日

3,5-Bis-trifluoromethylphenylboronic acid → 2-(3,5-Bis-trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one

https://huagongshe.com/ja/reaction/33299

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
反応物2-Phenyl-3,10-diazatricyclo[6.4.1.04,13]trideca-1,4,6,8(13)-tetraen-9-oneHCID 10220882—
生成物2-(3,5-Bis-trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-oneHCID 11014815—

反応手順

In a manner similar to that described for preparation of Compound 12, the tricyclic bromide (300 mg, 1.13 mmol) and 3,5-bis-trifluoromethylphenylboronic acid (202 mg, 1.24 mmol) were coupled to yield 2-(3,5-bis-trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one, 70 mg (16%), as a pale-yellow solid. mp 230° C. (dec.); 1H NMR (300 MHz, d6-DMSO) δ 3.11 (m, 2H), 3.42 (m, 2H), 7.31 (app t, 1H, J=7.8 Hz), 7.64 (d, 1H, J=8.1 Hz), 7.73 (d, 1H, J=7.5 Hz), 8.13 (br s, 1H), 8.16 (br t, 1H), 8.28 (br s, 2H), 11.95 (br s, 1H); MS (FAB, MH+) 399; Anal. (C19H12F6N2O.0.2 hexanes) C, H, N.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429578B2
出典データセットuspto-grants-2008_09
ORD IDord-4bcec7c6a83a40c7a6d14c93cbcee1e0
出典メモuspto-grants-2008_09