Sulfuric Acid → HCID 131727390, compound

HRID 874792Notes

Reaction equation

HRID 874792 reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[Cl:8][C:9]1[C:14]([Cl:15])=[C:13]([O:16][CH2:17][C@H:18]([OH:34])[CH2:19][NH:20][C:21]([CH3:33])([CH3:32])[CH2:22][CH:23]2[CH2:31][C:30]3[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=3)[CH2:24]2)[CH:12]=[CH:11][C:10]=1[CH:35]([CH2:39][CH:40]=[CH2:41])[C:36]([OH:38])=[O:37].S(=O)(=O)(O)O>C(O)C>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[CH2:2]([O:37][C:36](=[O:38])[CH:35]([C:10]1[CH:11]=[CH:12][C:13]([O:16][CH2:17][C@H:18]([OH:34])[CH2:19][NH:20][C:21]([CH3:33])([CH3:32])[CH2:22][CH:23]2[CH2:31][C:30]3[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=3)[CH2:24]2)=[C:14]([Cl:15])[C:9]=1[Cl:8])[CH2:39][CH:40]=[CH2:41])[CH3:3]

Participants

4

Procedure

The acid of Example 19 (0.5 g) was dissolved in absolute ethanol (10 mL) and catalytic amount of conc.sulfuric acid was added. The reaction was stirred and heated to reflux overnight. Next day the reaction was concentrated and diluted with ethyl acetate and washed with 2.5N NaOH (2×20 mL), brine (20 mL) and dried over sodium sulfate. The crude mixture was purified by HPLC (eluted with CH3CN/H2O containing 0.1% TFA) to produce the desired product in 81% yield (0.43 g). MS(ES) m/e 536 [M+H]+. 1H-NMR (400 MHz, DMSO-d6) δ: 8.35-8.48 (brs, 2H), 7.31-7.10 (m, 6H), 4.17-4.01 (m, 5H), 3.26-3.05 (m, 4H), 2.69-2.50 (m, 7H), 2.32 (t, 2H), 1.94 (d, 2H), 1.58-1.54 (t, 2H), 1.33 (s, 3H), 1.35 (s, 3H), 1.18 (t, 3H).

Workup

  1. temperatureheated
  2. temperatureto reflux overnight
  3. concentrationNext day the reaction was concentrated
  4. additiondiluted with ethyl acetate
  5. washwashed with 2.5N NaOH (2×20 mL), brine (20 mL)
  6. dry with materialdried over sodium sulfate
  7. customThe crude mixture was purified by HPLC (eluted with CH3CN/H2O containing 0.1% TFA)

Sources & evidence

ORD record
ord-7a3ca3074ec240c5909b9a48dd660f7a
Source dataset
uspto-grants-2015_03
Patent number
US08980950B2

Reaction notes

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