반응 #640613

ord-66e7debc52624f878cfa2ba7cf860426

반응 방정식

O=C1CCN2CCCC1C2.c1cc2cc(-c3cnc(O[C@H]4CCN5CCC[C@@H]4C5)nc3)ccc2[nH]1
(4S,5R)-4-[5-(1H-Indol-5-yl)-pyrimidin-2-yloxy]-1-aza-bicyclo[3.3.1]nonane 1-Aza-bicyclo[3.3.1]nonan-4-one
[BH4-].[Na+]
NaBH4
O
Water
OC1CCN2CCCC1C2
(4SR,5RS)-1-aza-bicyclo[3.3.1]nonan-4-ol
수율 91.0%

용매

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타does not exceed 0° C
  2. 2
    기타the solvents are evaporated
  3. 3
    workup.DISSOLUTIONThe remaining solid is dissolved in MTBE/MeOH
  4. 4
    여과filtered over hyflo
  5. 5
    기타the filtrate is evaporated
  6. 6
    기타to give 19.28 g of crude product which
  7. 7
    기타is purified by chromatography over aluminum oxide (400 g, eluent: MTBE/MeOH 95:5 to 80:20)

실험 절차

(4S,5R)-4-[5-(1H-Indol-5-yl)-pyrimidin-2-yloxy]-1-aza-bicyclo[3.3.1]nonane 1-Aza-bicyclo[3.3.1]nonan-4-one (11.92 g, 85.6 mmol) is dissolved in 160 ml MeOH and cooled to −10° C. NaBH4 (1.69 g, 42.9 mmol)) is added portionwise so that the inner temperature does not exceed 0° C. The reaction mixture is stirred at −10° C. for 1 h. Water is added and the solvents are evaporated. The remaining solid is dissolved in MTBE/MeOH, filtered over hyflo and the filtrate is evaporated to give 19.28 g of crude product which is purified by chromatography over aluminum oxide (400 g, eluent: MTBE/MeOH 95:5 to 80:20) to give 10.96 g (91%) (4SR,5RS)-1-aza-bicyclo[3.3.1]nonan-4-ol.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08048885B2uspto-grants-2011_11