반응식
[NH:1]1[CH2:6][CH2:5][S:4][CH2:3][C@H:2]1[C:7]([OH:9])=O.Cl[C:11]1[C:20]([N+:21]([O-])=O)=[CH:19][C:14]([C:15]([O:17][CH3:18])=[O:16])=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1.C(Cl)Cl.[Pt].[NH4+].[O-][V](=O)=O.P(OC1C=CC=CC=1)(OC1C=CC=CC=1)OC1C=CC=CC=1>[O:9]=[C:7]1[NH:21][C:20]2[CH:19]=[C:14]([C:15]([O:17][CH3:18])=[O:16])[CH:13]=[N:12][C:11]=2[N:1]2[CH2:6][CH2:5][S:4][CH2:3][C@@H:2]12참가 물질
반응물 3
생성물 1
시약·촉매·용매 5
실험 절차
To a suspension of (R)-thiomorpholine-3-carboxylic acid (1.009 g, 6.86 mmol) in THF was added methyl 6-chloro-5-nitronicotinate (1.35 g, 6.23 mmol) and potassium carbonate (2.58 g, 18.70 mmol). The suspension was heated to reflux for 3 hours. The crude orange solution was allowed to cool to RT and filtered through a pad of celite which was washed with DCM (50 mL), and transferred to a bomb hydroginator. To the solution was added triphenyl phosphite (0.019 ml, 0.061 mmol), platinum (0.238 g, 0.061 mmol), and ammonium metavanadate. The vessel was sealed and pressurized to 140 psi with stirring for 24 h at room temperature. The vessel was depressurized and the mixture was diluted with DCM (100 mL) and refluxed for 30 minutes. The hot mixture was filtered through celite and concentrated to yield 887 mg (52%) of the product as a white solid. [M+H] calc'd for C12H13N3O3S, 280; found, 280.
후처리
- temperatureThe suspension was heated
- temperatureto reflux for 3 hours
- filtrationfiltered through a pad of celite which
- washwas washed with DCM (50 mL)
- customThe vessel was sealed
- temperaturerefluxed for 30 minutes
- filtrationThe hot mixture was filtered through celite and
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-96ba58f6cfed4f7c9bc3834662e899d6
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08822470B2
연결된 노트
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