Diisopropylethylamine → 2-Allyl-5-(4-cyanophenyl)-7-methyl-3-oxo-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester
반응식
[CH3:1][O:2][C:3]([C:5]1[CH:6]([C:14]2[CH:19]=[CH:18][C:17]([C:20]#[N:21])=[CH:16][CH:15]=2)[N:7]=[C:8](OC)[NH:9][C:10]=1[CH3:11])=[O:4].Cl[C:23](OC1C=CC([N+]([O-])=O)=CC=1)=[O:24].Cl.[CH2:36]([NH:39][NH2:40])[CH:37]=[CH2:38].CCN(C(C)C)C(C)C>C(Cl)Cl.N1C=CC=CC=1.CC#N>[CH3:1][O:2][C:3]([C:5]1[CH:6]([C:14]2[CH:15]=[CH:16][C:17]([C:20]#[N:21])=[CH:18][CH:19]=2)[N:7]2[C:23](=[O:24])[N:39]([CH2:36][CH:37]=[CH2:38])[N:40]=[C:8]2[NH:9][C:10]=1[CH3:11])=[O:4]참가 물질
8
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 0 °C
실험 절차
Intermediate 4 (1.42 g, 5 mmol) was dissolved in a mixture of DCM (10 mL) and pyridine (10 mL) and cooled using an ice bath. A solution of 4-nitrophenyl chloroformate (0.955 mg, 4.75 mmol) in DCM (10 mL) was added dropwise, and the resulting solution was stirred at 0° C. for 1.5 hours, and then a solution of allyl hydrazine hydrochloride (1.0 g, 5.5 mmol) and DIPEA (3.75 mL, 22 mmol) in CH3CN (10 mL) was added in one portion. The resulting mixture was allowed to warm to RT, stirred for 4 hours, and then partitioned between EtOAc and water. The organic layer was separated, washed with water, followed by brine, then dried (Na2SO4) and evaporated in vacuo to yield the title compound as a yellow oil (0.95 g).
후처리
- temperaturecooled
- temperatureto warm to RT
- stirringstirred for 4 hours
- custompartitioned between EtOAc and water
- customThe organic layer was separated
- washwashed with water
- dry with materialdried (Na2SO4)
- customevaporated in vacuo
출처 및 근거
- ORD 기록
- ord-80cbf3ef0c9c402c8333f7f328b046c9
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08691826B2
반응 노트
불러오는 중…