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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1956788Erstellt: 27. Oktober 2026

Tert-butyl (piperidin-4-ylmethyl)carbamate → benzyl N-[4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]piperidine-1-carboximidoyl]carbamate

https://huagongshe.com/reaction/1956788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
EduktBenzyl [amino(methylsulfanyl)methylene]carbamateHCID 140362141—
LösungsmittelEthanolHCID 702—
Produktbenzyl N-[4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]piperidine-1-carboximidoyl]carbamateHCID 14039159737%

Reaktionsschritte

7.8 g (36.4 mmole) of 4-(N-tert-butyloxycarbonylaminomethyl) piperidine and 8.98 g (40 mmole) of N-benzyloxycarbonyl-S-methylisothiourea was mixed in 25 mL ethanol. The mixture was heated at 60°-70° C. for six hours and left at roomtemperature for two days. The solvent was evaporated and the residue was dissolved in CH2Cl2. The organic layer was washed twice with 0.3M KHSO4 and once with brine. The combined organic layer was dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography using a stepwise gradient of CH2Cl2 /MeOH (100/0, 97/3, 95/5, 90/10) as eluent to yield 5.22 g (37%) of the title product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05780631
Quelldatensatzuspto-grants-1998_07
ORD IDord-5176df8288004ce89412885e7a6f2da3
Quellennotizuspto-grants-1998_07