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HRID 1092476作成日:2026年10月25日

Water → (3aS,4R,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine

https://huagongshe.com/reaction/1092476

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriphenylphosphineHCID 11776—
反応物(3aS,4R,6aR)-4-azido-2-benzyloctahydrocyclopenta[c]pyrroleHCID 86641970—
溶媒TetrahydrofuranHCID 8028—
生成物(3aS,4R,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amineHCID 25918977—

反応条件

温度80 °C

反応手順

Triphenylphosphine (4.49 g, 17.13 mmol) and water (1.234 mL, 68.5 mmol) were added successively to a mixture of (3aS,4R,6aR)-4-azido-2-benzyloctahydrocyclopenta[c]pyrrole (1.384 g, 5.71 mmol) in tetrahydrofuran (30 mL). The reaction was refluxed at 80° C. for 2 hours. The crude material was adsorbed onto silica gel and applied to a silica gel cartridge (Analogix®, Burlington, Wis., RS-40) and eluted with 1-10% methanol (2 N ammonia)/chloroform to give (3aS,4R,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine: 1H NMR (500 MHz, pyridine-d5) δ ppm 7.45 (d, J=7.4, 2H), 7.38 (t, J=7.5, 2H), 7.29 (t, J=7.3, 1H), 3.52 (s, 2H), 3.14 (dd, J=5.7, 10.7, 1H), 2.62-2.55 (m, 1H), 2.52 (dd, J=3.2, 9.0, 1H), 2.38-2.29 (m, 3H), 2.20-2.13 (m, 1H), 2.01-1.84 (m, 2H), 1.40-1.29 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129417B2
出典データセットuspto-grants-2012_03
ORD IDord-f767667b5a1d464c839bd083e3192dc5
出典メモuspto-grants-2012_03