HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199565Generated: October 29, 2026
Diethyl azodicarboxylate → N-[3-(1-methylpiperidin-4-yl)-propyl]-N,N',N''-tri-Boc-guanidine
https://huagongshe.com/reaction/2199565
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | N,N',N''-Tri-Boc-guanidine | HCID 10570451 | — |
| Reactant | 3-(1-Methylpiperidin-4-yl)propan-1-ol | HCID 15540677 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(1-methylpiperidin-4-yl)-propyl]-N,N',N''-tri-Boc-guanidine | HCID 68526405 | — |
Reaction Steps
To a 100 mL, 3-neck, round bottom flask were added 3-(1-methyl -piperidin-4-yl)-propan-1-ol (1.91 g, 0.012 mol), Polymer Labs (Varian) PL-TPP resin (9.83 g, 0.014 mol), N,N′,N″-tri-Boc-guanidine (4.36 g, 0.012 mol) and THF (anhydrous, 100 mL). The resultant mixture was stirred and cooled to 2° C., at which time DEAD (2.53 g, 0.014 mol) was added drop wise over 10 min. Upon completion of addition, the flask was warmed to room temperature, aged for 4 h and filtered to remove the resin bound oxide. The resultant cake was rinsed with THF (25 mL) and heptane (2×25 mL). The filtrates were combined, extracted with saturated aqueous NaHCO3 (2×25 mL), dried over anhydrous MgSO4, filtered and concentrated. The resultant residue was triturated in hot ethanol (25 mL), cooled to room temperature and filtered. The filtrate was concentrated to yield N-[3-(1-methylpiperidin-4-yl)-propyl]-N,N′,N″-tri-Boc-guanidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359327B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4ae8ee25e19d49009718cb9734a69f57 |
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| Source note | uspto-grants-2016_06 |
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