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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1915972Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1915972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylamineHCID 8021—
EduktDiisopropylethylamineHCID 81531—
EduktFmoc-Gly-OHHCID 93124—
EduktPyBOPHCID 2724699—
Edukt{(R)-2-[(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionylamino]-3-methyl-butyrylamino}-acetic acid methyl esterHCID 57696983—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelAcetonitrile methylene chlorideHCID 21877088—
Produkt9H-fluoren-9-ylmethyl N-ethylcarbamate;methyl 2-[[1-[[(2S)-2-formamido-3-tritylsulfanylpropanoyl]amino]cyclopropanecarbonyl]amino]acetateHCID 86653402137,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08614193B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-48eb9fbe6dff47f5bc5c0937581b752b
Quellennotizuspto-grants-2013_12