戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 277873作成日:2026年10月25日

5-Bromo-4-methylthiophene-2-carbonitrile → 5-[4,4-Dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]-4-methylthiophene-2-carbonitrile

https://huagongshe.com/reaction/277873

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-4-methylthiophene-2-carbonitrileHCID 21986234—
反応物6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazineHCID 23435572—
生成物5-[4,4-Dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-6-yl]-4-methylthiophene-2-carbonitrileHCID 18374558—

反応手順

Prepared according to the coupling procedure for Example 13 from 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine and 5-bromo-4-methyl-2-thiophene-carbonitrile. A yellowish solid: mp 97-98° C.; 1H-NMR (DMSO-d6) δ 7.82 (s, 1H), 7.26 (d, 1H, J=1.7 Hz), 7.21 (dd, 1H, J=8.1, 2.1 Hz), 7.16 (s, 1H), 6.88 (d, 1H, J=8.1 Hz), 5.40 (m, 1H), 2.27 (s, 3H), 1.56 (s, 3H), 1.55 (s, 3H); MS (ESI) m/z 351 [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358948B1
出典データセットuspto-grants-2002_03
ORD IDord-4466bb8f32a14a3cab5ed59cf3e0e7a9
出典メモuspto-grants-2002_03