تفاعل #6528

ord-7c1e2ef533ec401fb17ad35bd72360ba

معادلة التفاعل

COC1O[C@H]2[C@H](OCc3ccccc3)[C@@H]1NC[C@@H]2OCc1ccccc1
amine
COC1O[C@H]2[C@H](OCc3ccccc3)[C@@H]1NC[C@@H]2OCc1ccccc1
Methyl 3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranoside
O=C([O-])O.[Na+]
sodium bicarbonate
O=C(Cl)OCc1ccccc1
benzylchloroformate
COC1O[C@H]2[C@H](OCc3ccccc3)[C@@H]1N(C(=O)OCc1ccccc1)C[C@@H]2OCc1ccccc1
Methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranoside

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe aqueous phase was then separated
  2. 2
    غسيلwashed with diethyl ether (3×10 ml)
  3. 3
    تجفيفThe combined ethereal layers were then dried (sodium sulphate)
  4. 4
    أخرىthe solvent removed in vacuo
  5. 5
    أخرىPurification by flash chromatography (0-50%, diethyl ether/hexane)

الإجراء التجريبي

To the crude amine (15), in a solution of diethyl ether:saturated sodium bicarbonate (3:2, 20 ml), was added benzylchloroformate (0.2 ml, 1.2 mmol). The reaction was then stirred, at such a rate as to make it one phase, for 2 hours. The aqueous phase was then separated and washed with diethyl ether (3×10 ml). The combined ethereal layers were then dried (sodium sulphate) and the solvent removed in vacuo. Purification by flash chromatography (0-50%, diethyl ether/hexane) then yielded methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-deoxy-2,6-imino-L-gulofuranoside (16), as a colorless oil (200 mg, 67% from azidotriflate). νmax (CHCl3): 1685, 750, 700 cm-1.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248779uspto-grants-1993_09