Реакция #541620

ord-83c90e1298e842c0bcb1664acd60a76e

Уравнение реакции

CCOC(=O)C1CC2(CN1)CN(C(=O)OC(C)(C)C)C2
2-(1,1-dimethylethyl) 7-ethyl 2,6-diazaspiro[3.4]octane-2,7-dicarboxylate
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
COC(=O)N[C@H](C(=O)O)C(C)C
N-[(methyloxy)carbonyl]-L-valine
CCN(C(C)C)C(C)C
Hunig's base
CCOC(=O)C1CC2(CN(C(=O)OC(C)(C)C)C2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
title compound
Выход 51.2%
CCOC(=O)C1CC2(CN(C(=O)OC(C)(C)C)C2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
2-(1,1-dimethylethyl) 7-ethyl 6-{N-[(methyloxy)carbonyl]-L-valyl}-2,6-diazaspiro[3.4]octane-2,7-dicarboxylate
Выход 51.2%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe reaction was concentrated in vacuo
  2. 2
    Другоеpurified by C18 reverse-phase chromatography
  3. 3
    Промывкаeluting with 10-90% ACN/water/0.2% NH4OH

Методика

To a solution of 2-(1,1-dimethylethyl) 7-ethyl 2,6-diazaspiro[3.4]octane-2,7-dicarboxylate (145) (500 mg, 1.76 mmol), HATU (735 mg, 1.93 mmol) and N-[(methyloxy)carbonyl]-L-valine (339 mg, 1.93 mmol) in anhydrous CH2Cl2 (10 mL) was added Hunig's base (0.68 mL, 3.87 mmol) and the reaction stirred at room temperature under nitrogen for 2 h. The reaction was concentrated in vacuo and purified by C18 reverse-phase chromatography eluting with 10-90% ACN/water/0.2% NH4OH to afford the title compound as an off-white solid (398 mg, 51% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08492554B2uspto-grants-2013_07