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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25700Generated: October 30, 2026

Diisopropylethylamine → 9H-fluoren-9-ylmethyl 11-[(3,3-diethoxypropyl)amino]-11-oxoundecyl-carbamate

https://huagongshe.com/reaction/25700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Amino-3,3-diethoxypropaneHCID 521029—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant11-amino-2-(9H-fluoren-9-ylmethoxycarbonyl)undecanoic acidHCID 54758961—
ReactantHCID 178418300HCID 178418300—
SolventTetrahydrofuranHCID 8028—
Product9H-fluoren-9-ylmethyl 11-[(3,3-diethoxypropyl)amino]-11-oxoundecyl-carbamateHCID 2075986523%

Reaction Steps

By using an analogous procedure to that described for Reference Example 13, Fmoc-11-aminoundecanoic acid (2 g, 4.7 mmol), hydroxybenzotriazole (639 mg, 4.7 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (906 mg, 4.7 mmol), 1-amino-3,3-diethoxypropane (662 gm, 4.5 mmol) and N,N-diisopropylethylamine (0.834 ml, 4.7 mmol) were reacted in anhydrous tetrahydrofuran (30 ml) at room temperature for 16 hours. Purification by chromatography (flash column, silica gel, 50-80% ethyl acetate in hexanes then 10% methanol in methylene chloride) provided 9H-fluoren-9-ylmethyl 11-[(3,3-diethoxypropyl)amino]-11-oxoundecyl-carbamate (560 mg, 23%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858591B2
Source datasetuspto-grants-2005_02
ORD IDord-1f2bee5318ed4281a52295de70ec8997
Source noteuspto-grants-2005_02