참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetralin | HCID 8404 | — |
| 반응물 | Ammonium formate | HCID 2723923 | — |
| 반응물 | 8-chloro-2-(N-n-propylamino)tetralin | HCID 14969229 | — |
| 반응물 | N-(Quinolin-3-Yl)propanamide | HCID 19032664 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-(N-Propionyl)amino-1,2,3,4-tetrahydroquinoline | HCID 19697664 | — |
반응 단계
To a solution of 17.4 g (86.9) 3-(N-propionyl)aminoquinoline and 20.0 g (317 mmol) ammonium formate in 150 ml methanol was added 1.0 g Pd/C cautiously under an inert atmosphere. After stirring at ambient temperature for 2 days the reaction stopped. The ratio between starting material and product was approximately 1:1 (monitored by GLC). The mixture was filtered on Celite and evaporated to a residue from which the product was extracted into diethyl ether. The ether solution was dried (magnesium sulfate), filtered and evaporated. The product/starting material mixture was then recharged in a similar manner using the same amounts of reactants. After additional 4 days the reaction was completed and worked-up as above to yield 9.7 g (55%) of reasonably pure material: MS m/e 204 (M+, 4), 130 (100), 131 (45), 118 (8), 91 (5), 77 (5).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05650427 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-731482a71cee432ba4e77138994a5a50 |
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| 출처 메모 | uspto-grants-1997_07 |
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