تفاعل #2271682

ord-b83a9d17e049439ba6fc72ccb4cde33e

معادلة التفاعل

Fc1ccc2c(C3CCNCC3)noc2c1
6-fluoro-3-(4-piperdinyl)-1,2-benzisoxazole
O=C([O-])[O-].[K+].[K+]
K2CO3
ClCCCOc1ccccc1
3-chloropropoxybenzene
CC#N
acetonitrile
Fc1ccc2c(C3CCN(CCCOc4ccccc4)CC3)noc2c1
6-fluoro-3-[1-(3-phenoxypropyl)-4-piperidinyl)-1,2-benzisoxazole
المردود 47.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux under nitrogen for 30 hours
  2. 2
    استخلاصthe aqueous mixture was extracted with ethyl acetate
  3. 3
    استخلاصThe ethyl acetate extract
  4. 4
    غسيلwas washed with brine
  5. 5
    أخرىdried with MgS04
  6. 6
    تركيزconcentrated
  7. 7
    أخرىto afford 6.2 g of a damp, beige solid
  8. 8
    أخرىThe compound was recrystallized twice from ethanol

الإجراء التجريبي

A mixture of 6-fluoro-3-(4-piperdinyl)-1,2-benzisoxazole (4.0 g, 18.2 mmol). K2CO3 (3.0 g, 21.8 mmol), Kl (100 mg), 3-chloropropoxybenzene (3.4 g, 20.0 mmol), and acetonitrile was stirred at reflux under nitrogen for 30 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate extract was washed with brine, dried with MgS04 and concentrated to afford 6.2 g of a damp, beige solid. The compound was recrystallized twice from ethanol to yield (47%) of 6-fluoro-3-[1-(3-phenoxypropyl)-4-piperidinyl)-1,2-benzisoxazole as a light beige solid, m.p.=78°-80° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE037729E1uspto-grants-2002_06