Trifluoroacetic acid → HCID 22730844, compound

HRID 2356080Notes

Reaction equation

HRID 2356080 reaction equation
[O:1]1CCCO[CH:2]1[CH2:7][CH2:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:45]=[CH:44][C:18]([C:19]([NH:21][S:22]([C:25]3[CH:30]=[CH:29][C:28]([NH:31][CH2:32][CH2:33][S:34][C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)=[C:27]([N+:41]([O-:43])=[O:42])[CH:26]=3)(=[O:24])=[O:23])=[O:20])=[CH:17][CH:16]=2)[CH2:11][CH2:10]1.C(O)(C(F)(F)F)=O>ClCCl.O>[N+:41]([C:27]1[CH:26]=[C:25]([S:22]([NH:21][C:19](=[O:20])[C:18]2[CH:44]=[CH:45][C:15]([N:12]3[CH2:11][CH2:10][CH:9]([CH2:8][CH2:7][CH:2]=[O:1])[CH2:14][CH2:13]3)=[CH:16][CH:17]=2)(=[O:24])=[O:23])[CH:30]=[CH:29][C:28]=1[NH:31][CH2:32][CH2:33][S:34][C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1)([O-:43])=[O:42]

Participants

5

Procedure

A solution of Example 203C (250 mg, 0.4 mmol), in dichloromethane (5 mL), TFA (1.5 mL), and 1 drop water was stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane, washed sequentially with water, saturated NaHCO3, and brine, dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with dichloromethane 0.5-1.0% methanol to provide the desired product. MS (APCI) m/e 597 (M+H)+; 1H NMR (300 MHz, CDCl3) δ 9.80 (s, 1H), 8.87 (d, 1H), 8.67 (t, 1H), 8.47 (s, 1H), 8.15 (dd, 1H), 7.63 (d, 2H), 7.40 (m, 2H), 7.24-7.34 (m, 4H), 6.87 (d, 2H), 6.82 (m, 2H), 3.87 (d, 2H), 3.58 (m, 4H), 3.21 (t, 2H), 2.86 (m, 2H), 2.50 (m, 2H), 1.80 (m, 2H), 1.62 (m, 2H), 1.55 (s, 4H) 1.31 (m, 2H).

Workup

  1. washwashed sequentially with water, saturated NaHCO3, and brine
  2. dry with materialdried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe concentrate was purified by flash column chromatography on silica gel with dichloromethane 0.5-1.0% methanol

Sources & evidence

ORD record
ord-53ec0c223981429d922dbcbb897e5c67
Source dataset
uspto-grants-2010_07
Patent number
US07754886B2

Reaction notes

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