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Trifluoroacetic acid → HCID 178494191, 화합물

HRID 2377971
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HRID 2377971 반응식
[I:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([O:8][CH3:9])[C:3]=1[C:10]1[NH:11][C:12]([C:16]([O:18]C(C)(C)C)=[O:17])=[C:13]([CH3:15])[N:14]=1.FC(F)(F)C(O)=O>ClCCl>[I:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([O:8][CH3:9])[C:3]=1[C:10]1[NH:11][C:12]([C:16]([OH:18])=[O:17])=[C:13]([CH3:15])[N:14]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 178494190HCID 178494190, 화합물

생성물 1

HCID 178494191HCID 178494191, 화합물수율 96%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A stirred solution of tert-butyl 2-(4-iodo-2-methoxypyridin-3-yl)-4-methyl-1H-imidazole-5-carboxylate (0.047 g, 0.1131 mmol) in dichloromethane (0.8 mL) was added trifluoroacetic acid (0.6 mL) and the reaction was stirred at room temperature overnight. The solvent was evaporated after adding toluene (1 mL) and the residue was purified on Prep HPLC (trifluoroacetic acid/acetonitrile/water) to give the title material (0.039 g, 96%). 1H NMR (400 MHz, MeOH-d4) δ (ppm): 2.70 (s, 3H) 3.97 (s, 3H) 7.70 (d, J=5.56 Hz, 1H) 8.11 (d, J=5.56 Hz, 1H).

후처리

  1. customThe solvent was evaporated
  2. additionafter adding toluene (1 mL)
  3. customthe residue was purified on Prep HPLC (trifluoroacetic acid/acetonitrile/water)

출처 및 근거

ORD 기록
ord-9288933b89804ab396840c73f5e1cbcb
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07470713B2

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