참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-(3-Chloropropoxy)-3-methoxyacetophenone | HCID 7314264 | — |
| 반응물 | 3-(4-Piperidinyl)-1,2-benzisoxazole Hydrochloride | HCID 13076437 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Desfluoro Iloperidone (Impurity) | HCID 10024423 | 47.7% |
반응 단계
A mixture of 3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (4.8 g, 20 mmol), K2CO3 (5.2 g, 40 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (5.3 g, 22 mmol), a few crystals of KI and dimethylformamide (60 ml) was stirred at 90 C. for 16 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The extract was washed (water), dried (MgSO4) and concentrated to afford a brown oil. The oil was chromatographed on a Waters Prep 500 utilizing silica gel columns and ethyl acetate-diethylamine (2%), as eluent. Concentration of the appropriate fractions afforded 3.9 g of product as an off-white solid. Recrystallization from absolute ethyl alcohol afforded 2.6 g (33%) of 1-[4-[3-[4-(1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxypehenyl]ethanone, m.p.=102°-104° C., as colorless needles.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05583145 |
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| 출처 데이터셋 | uspto-grants-1996_12 |
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| ORD ID | ord-6330f69fdb2b4bb5b9780888f1d9faa6 |
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| 출처 메모 | uspto-grants-1996_12 |
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