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HRID 1266081作成日:2026年10月27日

2-(Trifluoromethyl)benzeneboronic acid → tert-butyl (6aS,10aR)-2-[2-(trifluoromethyl)phenyl]4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)-carboxylate

https://huagongshe.com/reaction/1266081

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Trifluoromethyl)benzeneboronic acidHCID 2734387—
反応物Tert-butyl (6aS,10aR)-2-bromo-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)carboxylateHCID 20577007—
生成物tert-butyl (6aS,10aR)-2-[2-(trifluoromethyl)phenyl]4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)-carboxylateHCID 10003579—

反応手順

The title compound was prepared by the method of Example 89 step C from tert-butyl (6aS,10aR)-2-bromo-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH) carboxylate (189 mg, 0.5 mmol) and 2-(trifluoromethyl)phenylboronic acid (190 mg, 1.0 mmol) to afford after chromatographic purification the title compound (175 mg, 79%). 1H NMR (CDCl3, 300 MHz) δ7.69 (d, 1H, J=7.7 Hz), 7.50 (dd, 1H, J=7.3, 7.7 Hz), 7.40 (dd, 1H, J=7.7, 7.3 Hz), 7.31 (d, 1H, J=7.3 Hz), 6.89 (s, 1H), 6.85 (s, 1H), 3.82-4.30 (m, 2H), 3.66-3.71 (m, 1H), 2.88-3.50 (m, 7H), 1.80-1.90 (m, 2H), 1.47 (s, 9H) ppm. MS-ApCI: 445 [M+H+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06548493B1
出典データセットuspto-grants-2003_04
ORD IDord-f1cc23fdd78f4ac28e943abe13130ae7
出典メモuspto-grants-2003_04