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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(tert-Butoxycarbonyl)-1,5-diaminopentane | HCID 4352 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ste-Glu-AEEA-AEEA-OSU | HCID 86644536 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86674620 | HCID 86674620 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779109B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-e72c6f7b26fb4f4a801654788dce550e |
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| Source note | uspto-grants-2014_07 |
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