Реакция #41247

ord-922d3082846945a38837d1de7079dd7e

Уравнение реакции

CC(C)(C)[O-].[Na+]
sodium tert-butoxide
CC(C)(C)OC(=O)N1C[C@H]2CCN[C@H]2C1
tert-Butyl(3aR,6aR)-hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate
Brc1ccc(Br)cc1
1.4-dibromobenzene
c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1
BINAP
CC(C)(C)OC(=O)N1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
title compound
CC(C)(C)OC(=O)N1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
tert-Butyl(3aR,6aR)-1-(4-bromophenyl)hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate

Условия реакции

Температура
140°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеpurged three times with N2 gas
  2. 2
    workup.ADDITIONfollowed by the addition of toluene (45 mL)
  3. 3
    ТемператураThe mixture was then cooled to room temperature
  4. 4
    Фильтрацияwas filtered
  5. 5
    Другоеthe crude mixture was purified via chromatography (SiO2, 0-25% ethyl acetate:hexanes)

Методика

tert-Butyl(3aR,6aR)-hexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate (1, 1.5 g, 7.0 mmol), 1.4-dibromobenzene (2.8 g, 20.4 mmol), Pd2(dba)3 (275 mg, 0.3 mmol), BINAP (375 mg, 0.6 mmol) and sodium tert-butoxide (1.93 g, 20.0 mmol) were placed in glass microwave tubes and then purged three times with N2 gas, followed by the addition of toluene (45 mL). The mixture was heated to 140° C. for 15 minutes in a microwave reactor. The mixture was then cooled to room temperature, was filtered, and the crude mixture was purified via chromatography (SiO2, 0-25% ethyl acetate:hexanes) to provide the title compound. 1H NMR (300 MHz, CDCl3): δ=7.30 ppm (m, 2H), 7.39 (m, 2H), 4.11 (m, 1H), 3.57 (m, 3H), 3.31 (m, 3H), 2.99 (m, 1H), 2.15 (m, 1H), 1.92 (m, 1H), 1.43 (s, 9H). MS (ESI, M+1): 310.9.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728031B2uspto-grants-2010_06