تفاعل #2271670

ord-dc6e48974268438d830ea58e8f7c11df

معادلة التفاعل

Cl.Fc1ccc2c(C3CCNCC3)noc2c1
6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1cc(C(C)=O)ccc1OCCCCBr
1-[4-(4-bromobutoxy)-3-methoxyphenyl]ethanone
CN(C)C=O
dimethylformamide
COc1cc(C(C)=O)ccc1OCCCCN1CCC(c2noc3cc(F)ccc23)CC1
product
المردود 87.4%
COc1cc(C(C)=O)ccc1OCCCCN1CCC(c2noc3cc(F)ccc23)CC1
1-[4-[4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butoxy]-3-methoxyphenyl]ethanone
المردود 87.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe aqueous mixture was extracted with ethyl acetate
  2. 2
    غسيلThe ethyl acetate was washed (water)
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    تركيزthe solvent was concentrated
  5. 5
    أخرىto yield initially an oil, which
  6. 6
    أخرىThe solid was triturated with hexane
  7. 7
    أخرىcollected

الإجراء التجريبي

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (5.1 g, 0.02 mol). K2CO3 (5.2 g, 0.04 mol), 1-[4-(4-bromobutoxy)-3-methoxyphenyl]ethanone (6.6 g, 22 mmol), and dimethylformamide (60 ml) was heated a 75° C. for 5 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed (water), dried (MgSO4), and the solvent was concentrated to yield initially an oil, which solidified upon standing. The solid was triturated with hexane and collected to afford 7.7 g of the product as a waxy solid. The compound was chromatographed on a Waters Prep 500 utilizing silica gel columns and eluting with dichloromethane/methanol (5%). Concentration of the appropriate fractions yielded 5.1 g of off-white solid 1-[4-[4-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-butoxy]-3-methoxyphenyl]ethanone, which when recrystallized from ethyl alcohol yielded 3.2 g. (36%) of feathery white needles, m.p.=88°-90° C.

المصدر

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