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HRID 32464作成日:2026年10月24日

N-(9-Fluorenylmethoxycarbonyloxy)succinimide → n-[(r)-2-[(9h-Fluoren-9-ylmethoxycarbonyl)(1-isopropyl-piperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/32464

反応式

関与物質

役割名称HCID仕込み量
反応物N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
反応物N-[(R)-2-[(1-Isopropylpiperidin-4-ylmethyl)amino]-1-phenyl-ethyl]carbamic acid tert-butyl esterHCID 69307988—
生成物n-[(r)-2-[(9h-Fluoren-9-ylmethoxycarbonyl)(1-isopropyl-piperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl esterHCID 69309681113.5%

反応手順

Using coupling method B, N-[(R)-2-[(1-isopropylpiperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl ester (1.1 g, 2.8 mmol) and 9-fluorenylmethyl N-succinimidyl carbonate (Fmoc-OSu, 962 mg, 2.9 mmol) afforded 1.9 g of the title compound as a crude residue, that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427632B2
出典データセットuspto-grants-2008_09
ORD IDord-e4a11d44c2f74fedb928844e4d48c9a0
出典メモuspto-grants-2008_09