Diisopropylethylamine → tert-butyl N-[N-[2-methyl-2-(2,4,6-trimethylphenoxy)propanoyl]carbamimidoyl]carbamate

HRID 873778노트

반응식

HRID 873778 반응식
[C:1]1([CH3:16])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[O:9][C:10]([CH3:15])([CH3:14])[C:11]([OH:13])=O.C([N:20](C(C)C)CC)(C)C.N[N:27]([CH:35]=[NH:36])[C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:32])[CH3:31].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:20]=[C:35]([NH:27][C:28](=[O:34])[O:29][C:30]([CH3:33])([CH3:32])[CH3:31])[NH:36][C:11](=[O:13])[C:10]([O:9][C:2]1[C:1]([CH3:16])=[CH:6][C:5]([CH3:7])=[CH:4][C:3]=1[CH3:8])([CH3:15])[CH3:14]

참가 물질

8

실험 절차

2-(Mesityloxy)-2-methylpropionic acid (4.45 g; 20 mmol), diisopropylethylamine (12.93 g; 100 mmol), tert-butyl amino(imino)methylcarbamate (3.82 g; 24 mmol), and 1-hydroxybenzotriazole monohydrate (3.68 g; 24 mmol) were dissolved in N,N-dimethylformamide (100 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (9.10 g; 24 mmol) was added, and the mixture was stirred for 41 hours at room temperature. To the reaction solution, ethyl acetate (300 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 diisopropyl ether, collected by filtration and dried to give 4.82 g of the title compound (yield 66%).

후처리

  1. washthe mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. distillationdistilled under reduced pressure
  4. additionThe resulting crystals were dispersed in diisopropyl ether
  5. filtrationcollected by filtration
  6. customdried

출처 및 근거

ORD 기록
ord-c185fc7e81f24f6c87c8222ac8713be7
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08975411B2

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