Reaktion #167645

Reaktionsgleichung

HBTU

sodium

5-(benzyloxy)-2-({1-[(1,1-dimethylethoxy)carbonyl]piperidin-4-yl}[(2-methylpropoxy)carbonyl]amino)benzoic acid

DIEA

veratrylamine

→

expected product

1,1-Dimethylethyl 4-[{4-(benzyloxy)-2-[(3,4-dimethoxybenzyl)carbamoyl]phenyl}(isobutoxycarbonyl)amino]piperidine-1-carboxylate

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.WAITthe mixture is left
2. 2
   workup.STIRRINGstirring for 30 min
3. 3
   workup.STIRRINGthe reaction mixture is stirred for 48 h 00
4. 4
   SonstigeIt is evaporated under reduced pressure
5. 5
   Waschenwashed with a saturated NH4Cl solution and with a saturated NaHCO3 solution
6. 6
   Trocknendried over Na2SO4
7. 7
   Filtrationfiltered
8. 8
   Sonstigethe solvent is evaporated under reduced pressure
9. 9
   SonstigeThe residue is chromatographed on silica gel, elution

Vorschrift

A mixture of 6 g of sodium salt of 5-(benzyloxy)-2-({1-[(1,1-dimethylethoxy)carbonyl]piperidin-4-yl}[(2-methylpropoxy)carbonyl]amino)benzoic acid obtained in stage 1.3 and 4.42 g of DIEA in 250 ml of DMF is stirred at AT for 15 min. 6.48 g of HBTU are added and the mixture is left stirring for 30 min. 2.48 g of veratrylamine are added and the reaction mixture is stirred for 48 h 00. It is evaporated under reduced pressure, the residue is taken up in AcOEt, washed with a saturated NH4Cl solution and with a saturated NaHCO3 solution, dried over Na2SO4 and filtered, and the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel, elution being carried out with an AcOEt/heptane mixture, (20/80, v/v) as far as (60/40, v/v), to give 7.5 g of expected product.

Quelle