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Trifluoroacetic acid → 3-Amino-4-chloro-5-(4-hydroxybutan-2-yl)benzonitrile

HRID 921852
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반응식

HRID 921852 반응식
[Cl:1][C:2]1[C:7]([CH:8]([CH2:10][CH2:11][OH:12])[CH3:9])=[CH:6][C:5]([C:13]#[N:14])=[CH:4][C:3]=1[NH:15]C(=O)OC(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:15][C:3]1[CH:4]=[C:5]([CH:6]=[C:7]([CH:8]([CH2:10][CH2:11][OH:12])[CH3:9])[C:2]=1[Cl:1])[C:13]#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 131734941Tert-butyl (2-chloro-5-cyano-3-(4-hydroxybutan-2-yl)phenyl)carbamate

생성물 1

HCID 899224133-Amino-4-chloro-5-(4-hydroxybutan-2-yl)benzonitrile수율 127.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Tert-butyl (2-chloro-5-cyano-3-(4-hydroxybutan-2-yl)phenyl)carbamate (184 mg, 0.566 mmol) was taken up in DCM (6 mL) and TFA (1.746 mL, 22.66 mmol) was added. The reaction was stirred at room temperature for 1 h. LCMS indicates a mixture of the alcohol and the TFA ester. The solvent was removed in vacuo and the material dissolved in 2N NH3 in MeOH. The solution was stirred at room temperature for 10 min and the solvent removed in vacuo. 3-amino-4-chloro-5-(4-hydroxybutan-2-yl)benzonitrile (162 mg) was obtained. The crude material was taken forward without purification.

후처리

  1. customThe solvent was removed in vacuo
  2. dissolutionthe material dissolved in 2N NH3 in MeOH
  3. stirringThe solution was stirred at room temperature for 10 min
  4. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-69bc3f9d5939457d81890c815bc5dce1
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273057B2

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