HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193567Generated: October 31, 2026
N-(tert-Butoxycarbonyl)-1,5-diaminopentane → HCID 68525725, compound
https://huagongshe.com/reaction/2193567
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(tert-Butoxycarbonyl)-1,5-diaminopentane | HCID 4352 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionic Acid | HCID 21880607 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68525725 | HCID 68525725 | 118.2% |
Reaction Steps
A mixture of 3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionic acid (3 g, 8.15 mmol; prepared as described in Preparation 3), HATU (4.65 g, 12.2 mmol), N-tert-butoxycarbonyl-1,5-diaminopentane (2.47 g, 12.2 mmol) and DIPEA (4.25 mL, 24.52 mmol) in 100 mL of DCM was stirred at room temperature for 1 hour. The reaction mixture was washed with a 1:1 solution of brine and 1N HCl (100 mL), water (100 mL), dried over magnesium sulfate, filtered and concentrated. The residue was treated with 20% TFA in DCM (100 mL) at room temperature for 2 hours. The solvent and TFA were removed under reduced pressure. The residue was taken up in 100 mL of DCM and washed with 1N NaOH (100 mL) and brine (100 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated to give 4.36 g of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329911B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-d01ba166967b4d568fdbc150ef695f4f |
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| Source note | uspto-grants-2012_12 |
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