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Sodium Hydroxide → (5-(Cyano-dimethyl-methyl)-2-{3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-carbamic acid 2,2,2-trichloro-ethyl ester

HRID 2200051
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HRID 2200051 반응식
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH2:15][O:16][CH:17]3[CH2:22][CH2:21][CH2:20][CH2:19][O:18]3)[CH:8]=2)[N:5]=[C:4]([C:23]([CH3:27])([CH3:26])[C:24]#[N:25])[CH:3]=1.[OH-].[Na+].Cl[C:31]([O:33][CH2:34][C:35]([Cl:38])([Cl:37])[Cl:36])=[O:32]>CCOC(C)=O>[Cl:36][C:35]([Cl:38])([Cl:37])[CH2:34][O:33][C:31](=[O:32])[NH:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH2:15][O:16][CH:17]3[CH2:22][CH2:21][CH2:20][CH2:19][O:18]3)[CH:8]=2)[N:5]=[C:4]([C:23]([C:24]#[N:25])([CH3:27])[CH3:26])[CH:3]=1
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 870632,2,2-Trichloroethyl chloroformate3회HCID 1177287572-(5-Amino-1-{3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-1H-pyrazol-3-yl)-2-methyl-propionitrile

생성물 1

HCID 117729108(5-(Cyano-dimethyl-methyl)-2-{3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-phenyl}-2H-pyrazol-3-yl)-carbamic acid 2,2,2-trichloro-ethyl ester수율 80%

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

실험 절차

Intermediate 20c (317 mg, 0.86 mmol) was dissolved in EtOAc (2.5 mL) and 1M NaOH solution (1.4 mL, 2.14 mmol) and cooled in an ice bath. While stirring, 2,2,2-trichloroethyl chloroformate (227 mg, μL, 1.07 mmol) was then added dropwise, and the ice bath removed. After 30 min, a further 0.65 eq. of 2,2,2-trichloroethyl chloroformate was added, and the reaction continued. After 30 min, a further 0.65 eq. of 2,2,2-trichloroethyl chloroformate was added, and the reaction continued overnight. The reaction was then partitioned between H2O and EtOAc, the organic layer was separated, and the aqueous layer extracted again with EtOAc. The combined organics were dried over MgSO4, concentrated in vacuo and subjected to FCC, eluting with 5-30% EtOAc in cyclohexane, to afford the title compound as a light yellow oil (375 mg, 80%). LCMS (Method 3): Rt 4.41 min, m/z 567, 569 [M+Na].

후처리

  1. customthe ice bath removed
  2. waitAfter 30 min
  3. customthe reaction continued overnight
  4. customThe reaction was then partitioned between H2O and EtOAc
  5. customthe organic layer was separated
  6. extractionthe aqueous layer extracted again with EtOAc
  7. dry with materialThe combined organics were dried over MgSO4
  8. concentrationconcentrated in vacuo
  9. washeluting with 5-30% EtOAc in cyclohexane

출처 및 근거

ORD 기록
ord-9876eb4da6cd4002b81635d1c1cc20b6
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09359354B2

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