Diisopropylethylamine → tert-butyl N-[N-[2-(2,6-dimethylphenoxy)acetyl]carbamimidoyl]carbamate
반응식
[CH3:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([CH3:13])[C:3]=1[O:4][CH2:5][C:6]([OH:8])=O.C([N:17](C(C)C)CC)(C)C.N[N:24]([CH:32]=[NH:33])[C:25](=[O:31])[O:26][C:27]([CH3:30])([CH3:29])[CH3:28].O.ON1C2C=CC=CC=2N=N1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1>CN(C)C=O.C(OCC)(=O)C>[NH:17]=[C:32]([NH:24][C:25](=[O:31])[O:26][C:27]([CH3:30])([CH3:29])[CH3:28])[NH:33][C:6](=[O:8])[CH2:5][O:4][C:3]1[C:9]([CH3:13])=[CH:10][CH:11]=[CH:12][C:2]=1[CH3:1]참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
(2,6-Dimethylphenoxy)acetic acid (5.41 g; 30 mmol), diisopropylethylamine (19.39 g; 150 mmol), tert-butyl amino(imino)methylcarbamate (5.73 g; 36 mmol), and 1-hydroxybenzotriazole monohydrate (5.52 g; 36 mmol) were dissolved in N,N-dimethylformamide (120 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (13.66 g; 36 mmol) was added thereto, and the mixture was stirred for 65 hours at room temperature. To the reaction solution, ethyl acetate (400 mL) was added, and the mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution, and then brine. The organic layer was dried over anhydrous magnesium sulfate and then distilled under reduced pressure. The resulting crystals were dispersed in diethyl ether, collected by filtration and dried to give 9.03 g of the title compound (yield 94%).
후처리
- washthe mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- distillationdistilled under reduced pressure
- additionThe resulting crystals were dispersed in diethyl ether
- filtrationcollected by filtration
- customdried
출처 및 근거
- ORD 기록
- ord-320524c1c0524f128ac0d46c9b25fbe3
- 출처 데이터셋
- uspto-grants-2015_03
- 특허 번호
- US08975411B2
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