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Trimethyl orthoacetate → 3-Cyclohexyl-2-methyl-3H-imidazo[4,5-b]pyridin-5-ol

HRID 1890350
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HRID 1890350 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([OH:15])=[N:6][C:7]=1[NH:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1.[C:16](OC)(OC)(OC)[CH3:17]>C(O)(C(F)(F)F)=O>[CH:9]1([N:8]2[C:7]3=[N:6][C:5]([OH:15])=[CH:4][CH:3]=[C:2]3[N:1]=[C:16]2[CH3:17])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1
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참가 물질

4

반응물 2

HCID 15050Trimethyl orthoacetateHCID 178507771HCID 178507771, 화합물

생성물 1

HCID 1784322233-Cyclohexyl-2-methyl-3H-imidazo[4,5-b]pyridin-5-ol수율 5.4%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid촉매

실험 절차

5-Amino-6-(cyclohexylamino) pyridin-2-ol (0.1 g, 0.482 mmol) was dissolved in trimethyl orthoacetate (3.0 mL, 27.4 mmol). Several drops of TFA were added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated and the residues were diluted with water/acetonitrile (1:1). The mixture was purified via HPLC to give the title compound (0.006 g). LCMS m/z=232.30 [M+H]+; 1H NMR (400 MHz, methanol-d4) δ ppm 1.43-1.5 (m, 1H), 1.53-1.63 (m, 2H), 1.83 (d, J=11.87 Hz, 1H), 2.01 (d, J=10.99 Hz, 4H), 2.64-2.74 (m, 2H), 2.89 (s, 3H), 4.51-4.57 (m, 1H), 6.90 (d, J=8.8 Hz, 1H), 8.0 (d, J=8.8 Hz, 1H).

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additionthe residues were diluted with water/acetonitrile (1:1)
  3. customThe mixture was purified via HPLC

출처 및 근거

ORD 기록
ord-7899fc7758d54be3806011d7e271823b
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507473B2

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