Triethylamine → HCID 86677354, 화합물
반응식
[NH2:1][CH2:2][C:3]1[C:4](=[O:14])[NH:5][C:6]([CH:10]2[CH2:13][CH2:12][CH2:11]2)=[CH:7][C:8]=1[CH3:9].[NH2:15][CH2:16][C:17]1[C:18](=[O:28])[NH:19][C:20]([CH3:27])=[CH:21][C:22]=1[CH:23]1[CH2:26][CH2:25][CH2:24]1.CC([O:33][C:34](OC(OC(C)(C)C)=O)=[O:35])(C)C.C(N(CC)CC)C>C1COCC1.CN(C=O)C>[CH3:26][C:23]([N:1]([CH2:2][C:3]1[C:4](=[O:14])[NH:5][C:6]([CH:10]2[CH2:11][CH2:12][CH2:13]2)=[CH:7][C:8]=1[CH3:9])[C:34](=[O:33])[O-:35])([CH3:22])[CH3:24].[CH3:13][C:10]([N:15]([CH2:16][C:17]1[C:18](=[O:28])[NH:19][C:20]([CH3:27])=[CH:21][C:22]=1[CH:23]1[CH2:26][CH2:25][CH2:24]1)[C:34](=[O:33])[O-:35])([CH3:6])[CH3:11]참가 물질
반응물 4
생성물 2
시약·촉매·용매 2
반응 조건
- 온도
- 30 °C
실험 절차
To an ice bath cooled solution of 3-(aminomethyl)-6-cyclobutyl-4-methyl-2(1H)-pyridinone and 3-(aminomethyl)-4-cyclobutyl-6-methyl-2(1H)-pyridinone (3.5 g, 18 mmol) in THF (10 mL) and DMF (10 mL) were added Boc2O (4.68 g, 21.8 mmol) and triethylamine (5.4 g, 54 mmol). The contents were then stirred for 30 min. at 30° C. The reaction was quenched by addition of ice water, during which time precipitation occurred. The reaction mixture was filtered and dried to give a mixture of the crude products. The crude products were separated by HPLC to give 1,1-dimethylethyl[(6-cyclobutyl-4-methyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]carbamate (2.1 g, 20%) and 1,1-dimethylethyl[(4-cyclobutyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]carbamate (1 g, 9.5%). Data for 1,1-dimethylethyl[(6-cyclobutyl-4-methyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]carbamate:
후처리
- customThe reaction was quenched by addition of ice water, during which time precipitation
- filtrationThe reaction mixture was filtered
- customdried
- customto give
- customThe crude products were separated by HPLC
출처 및 근거
- ORD 기록
- ord-33566658c06e4049ba73b17aa098903c
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08536179B2
반응 노트
불러오는 중…