Hydrochloric Acid → Methyl 2-(4-((2-amino-4-(butylamino)-6-methylpyrimidin-5-yl)methyl)-3-hydroxyphenyl)acetate
반응식
[NH2:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[C:5]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]([OH:23])=[O:22])=[CH:16][C:15]=2[O:24]C)=[C:4]([CH3:26])[N:3]=1.[CH3:27]O.Cl>C(Cl)Cl.B(Br)(Br)Br.O1CCOCC1>[NH2:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[C:5]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]([O:23][CH3:27])=[O:22])=[CH:16][C:15]=2[OH:24])=[C:4]([CH3:26])[N:3]=1참가 물질
7
반응물 3
생성물 1
시약·촉매·용매 3
실험 절차
To the product from example 72 step (i) (550 mg) in DCM (20 mL), BBr3 (0.29 ml) was added dropwise and the reaction mixture stirred for 5 h. MeOH (4 mL) was added followed by 4M HCl in dioxane (0.5 mL) and stirred for 16 h and the solvents evaporated. The residue was purified by RPHPLC to give the title compound as a white solid, 8 mg.
후처리
- stirringstirred for 16 h
- customthe solvents evaporated
- customThe residue was purified by RPHPLC
출처 및 근거
- ORD 기록
- ord-a9a8e596245c416ba35482f0a56a6bc5
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765939B2
반응 노트
불러오는 중…