참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 4-(Benzoxazol-2-yl)benzyl bromide | HCID 11033515 | — |
| 반응물 | N-trityl-3-hydroxytricyclo-[3.3.1.13,7]decan-1-amine | HCID 54523384 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-trityl-3-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7]decan-1-amine | HCID 53730484 | — |
반응 단계
To KH (35%; 0.35 g; 0.003 mole) in THF (8 ml) under N2 and cooled to 0° C. is added N-trityl-3-hydroxytricyclo-[3.3.1.13,7 ]decan-1 -amine (1 g; 0.0025 mole) of all at once. The reaction is stirred for 5 minutes with ice cooling then at room temperature for an hour, developing into a clear yellow solution. Then 4-(benzoxazol-2-yl)benzyl bromide (0.70 g; 0.0025 mole) is added and the reaction cooled in ice for 10 minutes and stirred at room temperature for 4 hours. Methanol is added to quench any KH, then the reaction is filtered and evaporated to dryness. HPLC is used to purify the product (eluting with 10% ethyl acetate/hexane) to obtain N-trityl-3-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7 ]decan-1-amine (m.p. 174°-177° C.) which is used directly in step D.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05596020 |
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| 출처 데이터셋 | uspto-grants-1997_01 |
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| ORD ID | ord-826a2e324c84418a9ccc11a26eb0c153 |
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| 출처 메모 | uspto-grants-1997_01 |
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