Water → 8-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-6-methyl-2-(2-trifluoromethyl-phenyl)-7H-purine trifluoroacetic acid salt

HRID 1481575노트

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HRID 1481575 반응식
[NH2:1][C:2]1[C:3]([NH:19][C:20]([C:22]2[N:23]([CH3:31])[N:24]=[C:25]([C:27]([CH3:30])([CH3:29])[CH3:28])[CH:26]=2)=O)=[N:4][C:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]([F:18])([F:17])[F:16])=[N:6][C:7]=1[CH3:8].CC1(C)C2(CS(O)(=O)=O)C(CC1CC2)=[O:39].[OH2:47]>O1CCOCC1>[F:16][C:15]([F:18])([F:17])[C:10]([OH:39])=[O:47].[C:27]([C:25]1[CH:26]=[C:22]([C:20]2[NH:1][C:2]3[C:3](=[N:4][C:5]([C:9]4[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=4[C:15]([F:18])([F:17])[F:16])=[N:6][C:7]=3[CH3:8])[N:19]=2)[N:23]([CH3:31])[N:24]=1)([CH3:30])([CH3:29])[CH3:28]

참가 물질

5

반응물 3

HCID 962WaterHCID 18462Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 674110325-tert-butyl-2-methyl-2H-pyrazole-3-carboxylic acid [5-amino-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-amide

생성물 1

HCID 1363374478-(5-tert-Butyl-2-methyl-2H-pyrazol-3-yl)-6-methyl-2-(2-trifluoromethyl-phenyl)-7H-purine trifluoroacetic acid salt

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

A solution of 5-tert-butyl-2-methyl-2H-pyrazole-3-carboxylic acid [5-amino-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]-amide (45.8 mg, 0.106 mmol, prepared as described in the previous step) in 1,4-dioxane (10 mL) was treated with CSA (49.2 mg, 0.213 mmol) and heated to 100° C. under a reflux condenser for 3 h. The cooled mixture was then diluted with water (20 mL) and extracted twice with EtOAc (25 mL). The combined extracts were dried over MgSO4 and concentrated in vacuo. The residue was purified by RP-HPLC on a C18 column eluting with a linear gradient of 10-80% CH3CN in 0.1% TFA/H2O over 25 min to 8-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-6-methyl-2-(2-trifluoromethyl-phenyl)-7H-purine trifluoroacetic acid salt as an off-white solid. 1H-NMR (400 MHz, CD3OD) δ: 7.77 (d, J=7.6 Hz, 1H), 7.57-7.70 (m, 3H), 6.87 (s, 1H), 4.27 (s, 3H), 2.80 (s, 3H), 1.28 (s, 9H). Mass Spectrum (LCMS, APCI pos.): Calculated for C21H21F3N6: 415.2 (M+H). Measured: 415.2.

후처리

  1. extractionextracted twice with EtOAc (25 mL)
  2. dry with materialThe combined extracts were dried over MgSO4
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by RP-HPLC on a C18 column
  5. washeluting with a linear gradient of 10-80% CH3CN in 0.1% TFA/H2O over 25 min to 8-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-6-methyl-2-(2-trifluoromethyl-phenyl)-7H-purine trifluoroacetic acid salt as an off-white solid

출처 및 근거

ORD 기록
ord-8378ffcceb614dd696aa27c870d48271
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09409915B2

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