Trifluoroacetic acid → 6-((1R,2S)-2-amino-cyclohexylamino)-4-(1-methyl-1H-pyrazol-3-ylamino)-pyridazine-3-carboxylic acid amide

HRID 1396355노트

반응식

HRID 1396355 반응식
C([O:5]C(=O)[NH:7][C@H:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]1[NH:14][C:15]1[N:16]=[N:17][C:18]([C:28](=[O:30])[NH2:29])=[C:19]([NH:21][C:22]2[CH:26]=[CH:25][N:24]([CH3:27])[N:23]=2)[CH:20]=1)(C)(C)C.FC(F)(F)C(O)=O.C(=O)(O)[O-].[Na+]>ClCCl>[NH4+:7].[OH-:5].[NH2:7][C@H:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]1[NH:14][C:15]1[N:16]=[N:17][C:18]([C:28]([NH2:29])=[O:30])=[C:19]([NH:21][C:22]2[CH:26]=[CH:25][N:24]([CH3:27])[N:23]=2)[CH:20]=1

참가 물질

6

반응물 3

HCID 6422Trifluoroacetic acidHCID 516892Sodium BicarbonateHCID 86689723{(1S,2R)-2-[6-carbamoyl-5-(1-methyl-1H-pyrazol-3-ylamino)-pyridazin-3-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester

생성물 2

HCID 14923Ammonium HydroxideHCID 716268926-((1R,2S)-2-amino-cyclohexylamino)-4-(1-methyl-1H-pyrazol-3-ylamino)-pyridazine-3-carboxylic acid amide수율 38.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

{(1S,2R)-2-[6-carbamoyl-5-(1-methyl-1H-pyrazol-3-ylamino)-pyridazin-3-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (34 mg, 0.079 mmol) was dissolved in dichloromethane (1 mL) then cooled to 0° C. Trifluoroacetic acid (0.5 mL, 6.49 mmol) was added drop-wise then the reaction mixture was warmed to 25° C. After 4 h, the mixture was cooled in an ice bath and neutralized with sodium bicarbonate solution. The mixture was extracted with ethyl acetate, and the combined organic layers washed with brine, dried (sodium sulfate), filtered, and concentrated in vacuo. Purification by chromatography (silica, 0 to 80% of a 0.1:0.01 solution of methanol:NH4OH in dichloromethane) gave 6-((1R,2S)-2-amino-cyclohexylamino)-4-(1-methyl-1H-pyrazol-3-ylamino)-pyridazine-3-carboxylic acid amide (5 mg, 20%) as a brown solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 10.84-10.89 (m, 1H) 8.23-8.32 (m, 1H) 7.66 (d, J=2.3 Hz, 1H) 7.48-7.59 (m, 1H) 7.10 (s, 1H) 6.73 (d, J=7.9 Hz, 1H) 6.05 (d, J=2.3 Hz, 1H) 3.91-4.05 (m, 1H) 3.01-3.11 (m, 1H) 1.46-1.72 (m, 6H) 1.25-1.36 (m, 2H); LCMS (EI/CI) m/z: 331 [M+H].

후처리

  1. temperaturethe reaction mixture was warmed to 25° C
  2. temperaturethe mixture was cooled in an ice bath
  3. extractionThe mixture was extracted with ethyl acetate
  4. washthe combined organic layers washed with brine
  5. dry with materialdried (sodium sulfate)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification by chromatography (silica, 0 to 80% of a 0.1:0.01 solution of methanol

출처 및 근거

ORD 기록
ord-20735b72e5df4f55a617e084aee760f0
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08901124B2

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