Tetrahydrofuran → HCID 178504840, 화합물
반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:19]([OH:20])=[N:18][C:11]2[N:12]=[C:13](SC)[N:14]=[CH:15][C:10]=2[CH:9]=1.O[O:22][S:23]([O-:25])=O.[K+].O1CCC[CH2:28]1>O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:19]([OH:20])=[N:18][C:11]2[N:12]=[C:13]([S:23]([CH3:28])(=[O:25])=[O:22])[N:14]=[CH:15][C:10]=2[CH:9]=1참가 물질
5
실험 절차
To a solution of 6-(2-chlorophenyl)-2-methylthio-pyrido[2,3-d]pyrimidin-7-ol (25.2 g, 82.9 mmol) in 700 mL of tetrahydrofuran was added a slurry of Oxone™ (105 g, 171 mmol) in 200 mL of water. The reaction mixture was stirred for 5 hours, filtered, then concentrated in vacuo. The resulting slurry was filtered and the collected solid was washed with water and dried to give 23.2 g (83%) of 6-(2-chlorophenyl)-2-methanesulfonyl-pyrido[2,3-d]pyrimidin-7-ol (Sulfone 2) as a light-yellow solid. (mass spec. M+H+=336, mp=215.1-221.1° C.).
후처리
- filtrationfiltered
- concentrationconcentrated in vacuo
- filtrationThe resulting slurry was filtered
- washthe collected solid was washed with water
- customdried
출처 및 근거
- ORD 기록
- ord-1300dede526e4d41a8ae9cc4febd389a
- 출처 데이터셋
- uspto-grants-2003_01
- 특허 번호
- US06506749B2
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