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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624854Generated: October 31, 2026

N-(tert-Butoxycarbonyl)-1,5-diaminopentane → HCID 86674620, compound

https://huagongshe.com/reaction/1624854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
ReactantDiisopropylethylamineHCID 81531—
ReactantSte-Glu-AEEA-AEEA-OSUHCID 86644536—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86674620HCID 8667462055%

Reaction Steps

N-tert-butoxycarbonyl cadaverine (24.3 mg; 0.12 mmol) was added to a solution of 17-((S)-1-Carboxy-3-{2-[2-({2-[2-(2,5-dioxo-pyrrolidin-1-yloxycarbonyl methoxy)ethoxy]ethylcarbamoyl}methoxy)ethoxy]ethylcarbamoyl}propylcarbamoyl)-heptadecanoic acid (100 mg; 0.12 mmol) and DIPEA (46.68 mg; 0.36 mmol) in THF (2.0 ml). Reaction mixture was stirred over night at room temperature, and then concentrated in vacuo. The residue was dissolved in a mixture of water (5 ml) and THF (2 ml), and purified by preparative HPLC (RP18 column). Fractions containing the Boc-protected coupling product was pooled and taken to dryness. The residual was dissolved in 50% TFA-DCM (4 ml) and stirred for 1 h at room temperature, then concentrated in vacuo to provide 54 mg (55%) of the title material as its trifluoroacetic acid salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779109B2
Source datasetuspto-grants-2014_07
ORD IDord-e72c6f7b26fb4f4a801654788dce550e
Source noteuspto-grants-2014_07