Hydrochloric Acid → Toluene-4-thiosulfonic acid S-[2-tert-butyl-4-(4-cyano-benzenesulfonylamino)-5-methyl-phenyl] ester

HRID 1003875노트

반응식

HRID 1003875 반응식
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([S:9][S:10]([C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=2)(=[O:12])=[O:11])=[C:4]([C:20]([CH3:23])([CH3:22])[CH3:21])[CH:3]=1.[C:24]([C:26]1[CH:31]=[CH:30][C:29]([S:32](Cl)(=[O:34])=[O:33])=[CH:28][CH:27]=1)#[N:25].N1C=CC=CC=1.Cl>C(Cl)Cl>[C:20]([C:4]1[CH:3]=[C:2]([NH:1][S:32]([C:29]2[CH:28]=[CH:27][C:26]([C:24]#[N:25])=[CH:31][CH:30]=2)(=[O:34])=[O:33])[C:7]([CH3:8])=[CH:6][C:5]=1[S:9][S:10]([C:13]1[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=1)(=[O:12])=[O:11])([CH3:23])([CH3:22])[CH3:21]

참가 물질

6

실험 절차

A solution of toluene-4-thiosulfonic acid S-(4-amino-2-tert-butyl-5-methyl-phenyl) ester obtained from Example HHHH (0.20 g, 0.57 mmol), 4-cyanobenzenesulfonyl chloride (0.15 g, 0.74. mmol), pyridine (7 mL) and CH2Cl2 (1 mL) was stirred at room temperature under nitrogen overnight. 1N HCl was then added and the mixture was extracted with EtOAc. The organic phase was washed with 1N HCl and brine, dried (Na2SO4), filtered and concentrated. The resulting residue was flash chromatographed on silica gel, eluting with 19:1 CHCl3 :EtOAc to afford the title compound. 1H NMR (CDCl3) δ 1.16 (s, 9 H), 1.98 (s, 3 H), 2.43 (s, 3 H), 6.49 (s, 1 H), 7.23 (s, 1 H), 7.27 (d, partially obscured by CDCl3, 2 H), 7.48 (d, 2 H), 7.78 (d, 2 H), 7.87 (d, 2 H).

후처리

  1. extractionthe mixture was extracted with EtOAc
  2. washThe organic phase was washed with 1N HCl and brine
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customchromatographed on silica gel
  7. washeluting with 19:1 CHCl3

출처 및 근거

ORD 기록
ord-db902289ec1244b29370713f556758c2
출처 데이터셋
uspto-grants-2000_04
특허 번호
US06046355

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