Sulfuric Acid → 2-{[3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol-5-yl]amino}benzenesulfonamide

HRID 915603노트

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HRID 915603 반응식
C([N:8](CC1C=CC=CC=1)[S:9]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH:18][C:19]1[N:23]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[CH3:30])[N:22]=[C:21]([C:31]([CH3:34])([CH3:33])[CH3:32])[CH:20]=1)(=[O:11])=[O:10])C1C=CC=CC=1.OS(O)(=O)=O.[OH-].[Na+]>>[C:31]([C:21]1[CH:20]=[C:19]([NH:18][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[S:9]([NH2:8])(=[O:10])=[O:11])[N:23]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[CH3:30])[N:22]=1)([CH3:34])([CH3:33])[CH3:32]

참가 물질

4

실험 절차

N,N-Dibenzyl-2-{[3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol-5-yl]amino}benzene-sulfonamide (from Step 2, 240 mg, 0.42 mmol) was added to conc H2SO4 (3 mL), and the mixture was vigorously stirred for 20 min. The mixture was poured onto ice, and conc NaOH solution was added until a pH of ˜7.5 was reached. The aqueous layer was extracted 2× with EtOAc, and the combined organic layers were dried with Na2SO4, filtered, and concentrated under reduced pressure. Purification by silica gel flash chromatography using EtOAc/hexane (1:3, v/v) afforded the title compound as a white solid (104 mg, 64%). 1H NMR (δ 400 MHz, CD2Cl2) 61.39 (s, 9H), 2.09 (s, 3H), 4.50 (br, 2H), 6.20 (s, 1H), 7.94 (t, 1H), 7.23 (m, 4H), 7.34 (m, 2H), 7.45 (t, 1H), 7.73 (d, 1H). ES-MS m/z 385.2 (MH+); HPLC RT (min) 3.11.

후처리

  1. additionwas added until a pH of ˜7.5
  2. extractionThe aqueous layer was extracted 2× with EtOAc
  3. dry with materialthe combined organic layers were dried with Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customPurification by silica gel flash chromatography

출처 및 근거

ORD 기록
ord-46b46d649cfd424b97038400a8acb54f
출처 데이터셋
uspto-grants-2007_09
특허 번호
US07265144B2

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