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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352046Generated: October 26, 2026

Diethyl Ether → 2-(3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acid

https://huagongshe.com/reaction/1352046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Aminohexahydro-2-oxo-1H-azepine-1-acetic acidHCID 13749496—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-oxoazepan-1-yl)acetic acidHCID 471260398%

Reaction Steps

3-Aminohexahydro-2-oxo-1H-azepine-1-acetic acid (which can be prepared by the procedure of Thorsett, E. D. et al. J. Med. Chem. 1986, 29, 251–260; 9.3 g, 50 mmol) was added to a solution of sodium hydrogen carbonate (5 g, 60 mmol) in water (100 mL). A solution of 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy-2,5-pyrrolidinedione (Fmoc-Osu; 18.6 g, 55 mmol) in tetrahydrofuran (110 mL) was added. The solution was stirred at room temperature overnight and then ether (200 mL) was added. The layers were separated and the organic layer was back-extracted with saturated sodium hydrogen carbonate:water (1:1; 60 mL). The combined aqueous layers were acidified with 1 M HCl (110 mL). The solid was filtered off, washed with water (4×20 mL), and dried in vacuo to give 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]hexahydro-2-oxo-1H-azepine-1-acetic acid (20.1 g, 98%) as a white solid, mp 118° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217728B2
Source datasetuspto-grants-2007_05
ORD IDord-a3f7b82c32654be99f5791fbe9da1659
Source noteuspto-grants-2007_05