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HRID 1915972作成日:2026年10月27日

Diethylamine → 9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetate

https://huagongshe.com/reaction/1915972

反応式

関与物質

役割名称HCID仕込み量
反応物DiethylamineHCID 8021—
反応物DiisopropylethylamineHCID 81531—
反応物Fmoc-Gly-OHHCID 93124—
反応物PyBOPHCID 2724699—
反応物{(R)-2-[(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionylamino]-3-methyl-butyrylamino}-acetic acid methyl esterHCID 57696983—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
溶媒Acetonitrile methylene chlorideHCID 21877088—
生成物9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetateHCID 86653402137.6%

反応手順

To a solution of 1 (310.5 mg, 0.420 mmol) in MeCN/CH2Cl2 (10 mL/19 mL) under Ar(g) was added diethylamine (2.9 mL, 10% v/v) and the reaction mixture stirred at rt for 1 h 50 min. The solvent was removed in vacuo, the crude mixture treated with MeCN (3×20 mL) and the solvent was removed under reduced pressure. The crude amine was then dried under high vacuum for 1 h. Then to a solution of PyBOP (234.9 mg, 0.451 mmol) and FmocGly-OH (133.86 mg, 0.450 mmol) in CH2Cl2 (20 mL) was added diisopropylethylamine (0.25 mL, 1.44 mmol) under Ar(g) with stirring for 3 min. A solution of the resultant deprotected amine of 1 in MeCN (20 mL) was added, and the resulting mixture was allowed to stir at rt for 16 h. The solvent was then removed in vacuo. Purification by flash column chromatography on silica (eluant 1:99-3:97-5:95 MeOH/CH2Cl2) gave a white solid. The material was washed with 1M HCl (aq), dried (MgSO4) and concentrated in vacuo to give 2 (228.6 mg, 0.289 mmol, 68%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614193B2
出典データセットuspto-grants-2013_12
ORD IDord-48eb9fbe6dff47f5bc5c0937581b752b
出典メモuspto-grants-2013_12