반응식
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:11]([O:13][CH3:14])=[O:12])=[CH:7][NH:8]2)=[CH:4][C:3]=1B1OCC(C)(C)CO1.Br[C:24]1[CH:36]=[CH:35][C:27]([O:28][CH2:29][C@@H:30]2[CH2:34][CH2:33][CH2:32][NH:31]2)=[CH:26][CH:25]=1.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C>C1(C)C=CC=CC=1.C(O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([C:11]([O:13][CH3:14])=[O:12])=[CH:7][NH:8]2)=[CH:4][C:3]=1[C:24]1[CH:36]=[CH:35][C:27]([O:28][CH2:29][C@@H:30]2[CH2:34][CH2:33][CH2:32][NH:31]2)=[CH:26][CH:25]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 110 °C
실험 절차
A mixture of methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (80 mg, 0.146 mmol), (S)-2-((4-bromophenoxy)methyl)pyrrolidine (77 mg, 0.3 mmol), 2.0M aqueous potassium carbonate (0.5 mL, 1.0 mmol), and Pd(dppf)Cl2 (10 mg, 0.01 mmol) in toluene/ethanol (1.44 mL/0.48 mL) was stirred at 110° C. for 2.5 hours. The mixture was poured into ethyl acetate and washed with water. The organic phase was dried over sodium sulfate, filtered, and concentrated to give a residue, which was purified by preparative TLC to give the title compound (40 mg, 42% yield) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.92 (s, 1H), 7.80 (s, 1H), 7.55 (s, 1H), 7.45 (d, 2H), 6.85 (d, 2H), 4.10 (m, 1H), 3.75 (s, 3H), 3.65 (m, 1H), 3.52 (m, 1H), 3.05 (m, 2H), 2.05 (m, 1H), 1.90 (m, 2H), 1.70 (m, 1H).
후처리
- washwashed with water
- dry with materialThe organic phase was dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a residue, which
- customwas purified by preparative TLC
출처 및 근거
- ORD 기록
- ord-1d14a0a227144f08b234103ddb568383
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889730B2
연결된 노트
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