반응식
F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.[I:23][C:24]1[CH:32]=[CH:31][C:27]([C:28]([OH:30])=O)=[CH:26][CH:25]=1.C(N(C(C)C)C(C)C)C.[C:42]([O:46][C:47]([N:49]1[CH2:54][CH2:53][CH:52]([NH:55][CH:56]2[CH2:58][CH2:57]2)[CH2:51][CH2:50]1)=[O:48])([CH3:45])([CH3:44])[CH3:43]>CN(C)C=O>[C:42]([O:46][C:47]([N:49]1[CH2:54][CH2:53][CH:52]([N:55]([CH:56]2[CH2:57][CH2:58]2)[C:28](=[O:30])[C:27]2[CH:26]=[CH:25][C:24]([I:23])=[CH:32][CH:31]=2)[CH2:51][CH2:50]1)=[O:48])([CH3:45])([CH3:43])[CH3:44]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (2.67 g) is added to a solution of 4-iodo-benzoic acid (2.06 g) and ethyldiisopropylamine (2.88 mL) in N,N-dimethylformamide (15 mL) at room temperature. The solution is stirred for 10 min prior to the addition of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (2.00 g). The resulting mixture stirred at room temperature overnight. The mixture is concentrated in vacuo and the residue is mixed with water and ethyl acetate. The organic phase is separated, washed with water and aqueous NaHCO3 solution, dried, and the solvent is evaporated. The crude product is used for the next reaction step without further purification. LC (method 5): tR=2.32 min; Mass spectrum (ESI+): m/z=471 [M+H]+.
후처리
- stirringThe resulting mixture stirred at room temperature overnight
- concentrationThe mixture is concentrated in vacuo
- additionthe residue is mixed with water and ethyl acetate
- customThe organic phase is separated
- washwashed with water and aqueous NaHCO3 solution
- customdried
- customthe solvent is evaporated
- customThe crude product is used for the next reaction step without further purification
출처 및 근거
- ORD 기록
- ord-464cde27ee4d4693b998c15da72b5346
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08822471B2
연결된 노트
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