tert-Butyl cyanoacetate → Tert-butyl 2-amino-4-{1-[(benzyloxy)carbonyl]-3-piperidinyl}-6-{2-[(4-methoxybenzyl)oxy]phenyl}nicotinate

HRID 412263

반응식

HRID 412263 반응식
[CH3:1][O:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15](=O)[CH3:16])=[CH:5][CH:4]=1.[CH:20]([CH:22]1[CH2:27][CH2:26][CH2:25][N:24]([C:28]([O:30][CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[O:29])[CH2:23]1)=O.[C:38]([CH2:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])#[N:39].C([O-])(=O)C.[NH4+:52]>COCCOC>[NH2:39][C:38]1[N:52]=[C:15]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[O:8][CH2:7][C:6]2[CH:18]=[CH:19][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[CH:16]=[C:20]([CH:22]2[CH2:27][CH2:26][CH2:25][N:24]([C:28]([O:30][CH2:31][C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[O:29])[CH2:23]2)[C:40]=1[C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42]

참가 물질

6

반응물 4

HCID 70693tert-Butyl cyanoacetateHCID 517165Ammonium AcetateHCID 9899653Benzyl 3-formylpiperidine-1-carboxylate2회HCID 98998251-{2-[(4-Methoxybenzyl)oxy]phenyl}ethanone2회

생성물 1

HCID 10232833Tert-butyl 2-amino-4-{1-[(benzyloxy)carbonyl]-3-piperidinyl}-6-{2-[(4-methoxybenzyl)oxy]phenyl}nicotinate수율 14.2%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A solution of 1-{2-[(4-methoxybenzyl)oxy]phenyl}ethanone (14.2 g, 55.4 mmol)(starting compound 1D), benzyl 3-formyl-1-piperidinecarboxylate (13.7 g, 55.4 mmol)(starting compound 2C), tert-butyl cyanoacetate (7.8 g, 55.4 mmol), and ammonium acetate (9.8 g, 166.1 mmol) in 1,2-dimethoxyethane (60 mL) was stirred under reflux for 3.5 hrs. After cooled to room temperature, the mixture was partitioned between ethyl acetate and water. The separated organic phase was washed with water and brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane, 1:2) to give tert-butyl 2-amino-4-{1-[(benzyloxy)carbonyl]-3-piperidinyl}-6-{2-[(4-methoxybenzyl)oxy]phenyl}nicotinate as a pale yellow oil (4.89 g, yield; 14%).

후처리

  1. temperatureunder reflux for 3.5 hrs
  2. customthe mixture was partitioned between ethyl acetate and water
  3. washThe separated organic phase was washed with water and brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel (ethyl acetate:hexane, 1:2)

출처 및 근거

ORD 기록
ord-be01eb3ae7bc4fa28a36ba7b61adb182
출처 데이터셋
uspto-grants-2003_05
특허 번호
US06562811B1

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