반응식
[NH2:1][C:2]1[C:12](I)=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[C:4]([Cl:14])[CH:3]=1.[C:15]([OH:20])(=[O:19])[C:16]([CH3:18])=O.N12CCN(CC1)CC2>CN(C)C=O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:14][C:4]1[CH:3]=[C:2]2[C:12]([CH:18]=[C:16]([C:15]([OH:20])=[O:19])[NH:1]2)=[CH:11][C:5]=1[C:6]([O:8][CH2:9][CH3:10])=[O:7]참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
A solution of ethyl 4-amino-2-chloro-5-iodobenzoate (1.82 g, 5.59 mmol) in N,N-dimethylformamide (18 ml) under argon was admixed with pyruvic acid (1.27 ml, 18.2 mmol) and 1,4-diazabicyclo[2.2.2]octane, evacuated and flooded with argon. Then argon was passed through the solution for 5 min, and then palladium(II) acetate (68 mg, 0.30 nmol) was added and the mixture was heated to 100° C. for 2 h. The cooled solution was filtered through Celite and the filtercake was rinsed with ethyl acetate (100 ml). The filtrate (suspension) was washed with hydrochloric acid (2 M; 2×25 ml) and with water (2×25 ml), dried over sodium sulphate and filtered. The filtrate was concentrated to dryness under reduced pressure and gives a red-brown solid (1.93 g, approx. 51% product), which was used for the next step without further purification.
후처리
- customevacuated
- filtrationThe cooled solution was filtered through Celite
- washthe filtercake was rinsed with ethyl acetate (100 ml)
- washThe filtrate (suspension) was washed with hydrochloric acid (2 M; 2×25 ml) and with water (2×25 ml)
- dry with materialdried over sodium sulphate
- filtrationfiltered
- concentrationThe filtrate was concentrated to dryness under reduced pressure
출처 및 근거
- ORD 기록
- ord-492390ccdc7c4fcfa7ebd7e09b8a8673
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08710242B2
연결된 노트
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