Water → Methyl 6-(trifluoromethyl)-1H-indazole-3-carboxylate

HRID 1809327노트

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HRID 1809327 반응식
[CH3:1][O:2][C:3](=[O:19])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][C:6]=1[NH:15]C(=O)C.[N:20](OC(C)(C)C)=O.O>C(O)(=O)C>[CH3:1][O:2][C:3]([C:4]1[C:5]2[C:6](=[CH:7][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:9][CH:10]=2)[NH:15][N:20]=1)=[O:19]

참가 물질

5

반응물 3

HCID 962WaterHCID 10906Tert-Butyl nitriteHCID 57633614(2-Acetylamino-4-trifluoromethylphenyl)-acetic acid methyl ester

생성물 1

HCID 53408454Methyl 6-(trifluoromethyl)-1H-indazole-3-carboxylate

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
95 °C

실험 절차

To a solution of (2-acetylamino-4-trifluoromethylphenyl)-acetic acid methyl ester (16 g, 0.058 mol) in acetic acid (50 mL) was added dropwise t-butyl nitrite (90%) (7.35 g, 0.063 mol) over a period of 20 min. at 90-95° C. The mixture was then stirred for 0.5 h at 95° C., poured into cold water and stirred for 1 h. The precipitates were collected by filtration and washed with water. The crude material was dissolved in ethyl acetate and dried over sodium sulfate. The solvent was removed in vacuo. This material (13.4 g, 95%) was used without further purification in the next step. A small sample was crystallized from ethyl acetate to yield a white solid, mp 240-242° C. 1H NMR (DMSO-d-6) 8.25 (d, J=8.5 Hz, 1H), 8.04 (s, 1H), 7.58 (d, J=8.5 Hz, 1H), 3.95 (s, 3H). MS (FAB) m/z: 245.1 (M++1).

후처리

  1. stirringstirred for 1 h
  2. filtrationThe precipitates were collected by filtration
  3. washwashed with water
  4. dissolutionThe crude material was dissolved in ethyl acetate
  5. dry with materialdried over sodium sulfate
  6. customThe solvent was removed in vacuo
  7. customThis material (13.4 g, 95%) was used without further purification in the next step
  8. customA small sample was crystallized from ethyl acetate
  9. customto yield a white solid, mp 240-242° C

출처 및 근거

ORD 기록
ord-3b6e969c89444c77bab8736369acc103
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362031B2

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