تفاعل #2254224

ord-7d99ca31b0324fe1bf6406180db7acf3

معادلة التفاعل

[Al+3].[H-].[H-].[H-].[H-].[Li+]
LAH
N#CC[C@@]1(c2ccccn2)CCOC2(CCCC2)C1
2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]acetonitrile
NCC[C@@]1(c2ccccn2)CCOC2(CCCC2)C1
2-[(9R)-9-(Pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]ethan-1-amine
المردود 94.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe resulting mix
  2. 2
    درجة الحرارةThe reaction was cooled at 0° C.
  3. 3
    أخرىquenched with water (1.12 ml), NaOH (10%, 2.24 ml)
  4. 4
    ترشيحSolid was filtered
  5. 5
    ترشيحfilter pad
  6. 6
    غسيلwas washed with ether (3×20 ml)
  7. 7
    أخرىThe combined organic was dried
  8. 8
    تركيزconcentrated

الإجراء التجريبي

LAH (1M in Et2O, 20 ml, 20 mmol) was added to a solution of 2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]acetonitrile (2.56 g, 10 mmol) in Et2O (100 ml, 0.1M) at 0° C. under N2. The resulting mix was stirred and allowed to warm to room temperature. After 2 h, LCMS showed the reaction had completed. The reaction was cooled at 0° C. and quenched with water (1.12 ml), NaOH (10%, 2.24 ml) and another 3.36 ml of water. Solid was filtered and filter pad was washed with ether (3×20 ml). The combined organic was dried and concentrated to give 2-[(9R)-9-(Pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]ethan-1-amine (2.44 g, 94% yield, m/z 260.6 [M+H]+ observed) as a light amber oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09044469B2uspto-grants-2015_06