Réaction #1246

ord-48ed68423d4a4e7fb6e576167938191c

Équation de réaction

c1ccncc1
pyridine
CC(C)(C)[Si](C)(C)Cl
TBDMSCl
N[C@H](CO)Cc1c[nH]cn1
histidinol
[H-].[Na+]
NaH
Cl.Cl.N[C@H](CO)Cc1c[nH]cn1
histidinol dihydrochloride
ClCCl.N
NH3 CH2Cl2
N[C@H](CO)Cc1c[nH]cn1
14
N[C@H](CO)Cc1c[nH]cn1
histidinol

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreresulting in moderate gas evolution
  2. 2
    workup.STIRRINGThe solution was stirred for 1.5 h
  3. 3
    Concentrationconcentrated in vacuo and flash
  4. 4
    Autrechromatographed on silica with 15% CH3OH

Mode opératoire

TBDMS protected histidinol 14--To a stirred solution of 205 mg (5.1 mmol) of NaH washed 3× with hexane, under argon, in 3.0 mL DMF was added in portions 500 mg (2.3 mmol) of histidinol dihydrochloride, resulting in moderate gas evolution. The solution was stirred for 1.5 h, then 1.8 mL (23 mmol) of anhydrous pyridine and 693.0 mg (4.6 mmol) of TBDMSCl was added. The solution was stirred for 1.5 h, concentrated in vacuo and flash chromatographed on silica with 15% CH3OH.NH3 /CH2Cl2 to yield 14.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723592uspto-grants-1998_03