Réaction #487548

ord-a306553d7b024c76aa40148fcf6f7e78

Équation de réaction

O=C(Nc1ccc2c(c1)CCNC2)OCc1ccccc1
benzyl (1,2,3,4-tetrahydro-isoquinolin-6-yl)-carbamate
O=C([O-])O.[Na+]
sodium hydrogen carbonate
C=O
formalin
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
sodium triacetoxyborohydride
O=C([O-])C(F)(F)F
trifluoroacetate
CN1CCc2cc(NC(=O)OCc3ccccc3)ccc2C1
benzyl (2-methyl-1,2,3,4-tetrahydro-isoquinolin-6-yl)-carbamate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGthe mixture is stirred for two hours
  2. 2
    Extractionextracted three times with ethyl acetate
  3. 3
    AutreThe combined organic phases are dried on sodium sulphate
  4. 4
    Autreevaporated to dryness i.vac

Mode opératoire

1.5 g (3.8 mmol) benzyl (1,2,3,4-tetrahydro-isoquinolin-6-yl)-carbamate (as the trifluoroacetate salt) are suspended in 8 ml of methanol and adjusted to pH 6 with acetic acid. 0.6 ml (8.5 mmol) formalin solution (37% in water) are added and the mixture is stirred for 30 minutes at RT. Then a total of 1.8 g (8.5 mmol) sodium triacetoxyborohydride are added batchwise and the mixture is stirred for two hours. The reaction mixture is poured onto sat. sodium hydrogen carbonate solution and extracted three times with ethyl acetate. The combined organic phases are dried on sodium sulphate and evaporated to dryness i.vac.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08741890B2uspto-grants-2014_06