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HRID 449755作成日:2026年10月24日

2,5-Dimethoxytetrahydrofuran → (S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoate

https://huagongshe.com/ja/reaction/449755

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-DimethoxytetrahydrofuranHCID 79098—
反応物methyl (2S)-2-amino-6-(phenylmethoxycarbonylamino)hexanoateHCID 6994982—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物(S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoateHCID 6799316649.5%

反応条件

温度110 °C

反応手順

A vigorously stiffed solution of L-Lys(Z)—OMe (3.31 g, 10 mmol) in acetic acid (20 mL) and dioxane (40 mL) was heated to 75° C., at this temperature 2,5-dimethoxytetrahydrofuran (DMTHF, ee 97%) (3.97 g, 3.90 mL, 30 mmol) was added dropwise to the reaction mixture. After complete addition of DMTHF, the reaction mixture was refluxed at 110° C. for 3 h followed by 5-6 h stiffing at room temperature. The volatiles were removed under reduced pressure to afford a dark brown residue, which was dissolved in dichloromethane (100 mL) and washed with 10% NaHCO3 solution (15 mL), brine (15 mL) and water (15 mL). The organic phase was dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (230-400 mesh) using hexane:ethyl acetate (7:3) as eluent to afford (S)-methyl 6-benzyloxycarbonylamino-2-carbazol-9-yl-hexanoate 3 (1.10 g, 25%) as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486534B2
出典データセットuspto-grants-2013_07
ORD IDord-6d9649b7421447f4a7a6b7819e714072
出典メモuspto-grants-2013_07