참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 6-Bromo-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthalene | HCID 10039346 | — |
| 반응물 | 3-acetyl-2-pyridinecarboxylic acid N,N-diisopropylamide | HCID 53662512 | — |
| 생성물 | 2-Pyridinecarboxamide | HCID 15070 | 80% |
반응 단계
2-Bromo-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalene 33 (620 mg, 2.2 mmol) and the acetylpyridineamide 36a (500 mg, 2 mmol) were converted by a similar method as described above to obtain the intermediate 34 in over 80% yield. To a solution of the pyridine amide 34 (432 mg, 1 mmol) in 5 mL of THF at −78° C. was added 1.5 M DIBAL toluene solution (0.7 mL, 1.05 mmol) and the resulting yellow clear solution was warmed up to −20° C. slowly in 60 min. and then was quenched with water. Removal of solvent and chromatography of the crude mixture afforded the pyridinealdehyde 35 in 83% yield as a white solid. 1H-NMR (CDCl3) δ1.25 (s,2(CH3)), 1.29 (s,2(CH3)), 1.70 (s,2(CH2)), 1.96 (s,CH3), 5.47 (s,═CH), 5.92 (s,═CH), 7.10 (s,Ar—CH), 7.11 (s,Ar—CH), 7.70 (d,J=8.0 Hz,Pyr—CH), 7.88 (d,J=8.0 Hz,Pyr—CH), 8.72 (s, Pyr—CH), 10.06 (s,CHO).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06320074B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-3015c289f4fc44a4880cea8d8041a58c |
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| 출처 메모 | uspto-grants-2001_11 |
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