반응식
[CH3:1][N:2]1[C:7]2=[CH:8][N:9]([CH2:19][CH2:20][S:21]C(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)[C:10]([C:11]3[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=3)[C:14]#[N:15])=[C:6]2[C:5](=[O:41])[N:4]([CH3:42])[C:3]1=[O:43].CSC1NC(=S)NC(=S)N=1.C([SiH](CC)CC)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[SH:21][CH2:20][CH2:19][N:9]1[C:10]([C:11]2[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=2)[C:14]#[N:15])=[C:6]2[C:7]([N:2]([CH3:1])[C:3](=[O:43])[N:4]([CH3:42])[C:5]2=[O:41])=[CH:8]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
3-(1,3-Dimethyl-2,4-dioxo-6-(2-(tritylthio)ethyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)benzonitrile (step 1)(573 mg, 0.983 mmol) was dissolved in DCM (20 ml) to form a clear brown solution and passed through 2×500 mg Isolute® Si-TMT (silica bound equivalent of 2,4,6-trimercatotriazine) cartridges to afford a colourless solution. The solution was placed under a nitrogen atmosphere and whilst stirring rapidly, treated dropwise with triethylsilane (1.571 ml, 9.83 mmol) followed TFA (3.79 ml, 49.2 mmol). After stirring at RT for 1 h, the reaction mixture was concentrated under reduced pressure to yield a white solid. The isolated crude product was triturated with diethyl ether and dried in a vacuum oven at 50° C. to afford the title compound;
후처리
- customto form a clear brown solution
- customto afford a colourless solution
- stirringAfter stirring at RT for 1 h
- concentrationthe reaction mixture was concentrated under reduced pressure
- customto yield a white solid
- customThe isolated crude product
- customwas triturated with diethyl ether
- customdried in a vacuum oven at 50° C.
출처 및 근거
- ORD 기록
- ord-88988c59cc494c8d9684180980f01e6f
- 출처 데이터셋
- uspto-grants-2016_06
- 특허 번호
- US09359381B2
연결된 노트
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