Hydrochloric Acid → HCID 67593614, compound

HRID 1379144Notes

Reaction equation

HRID 1379144 reaction equation
[Cl:1][CH:2]1[S:7][C:6]2[S:8][CH:9]=[CH:10][C:5]=2[C:4](=[O:11])[CH2:3]1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[F:22][C:23]([F:32])([F:31])[C:24](C1NC=CN=1)=[O:25].Cl>O1CCCC1>[Cl:1][CH:2]1[S:7][C:6]2[S:8][CH:9]=[C:10]([C:24](=[O:25])[C:23]([F:32])([F:31])[F:22])[C:5]=2[C:4](=[O:11])[CH2:3]1

Participants

6

Conditions

Temperature
-78 °C

Procedure

The compound from Step 3 (1.03 g, 5.0 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to -78° C. A solution of sodium bistrimethylsilylamide (5.0 mL of a 1.0M tetrahydrofuran solution) was added and the reaction stirred for 0.75 hours at -78° C. Trifluoroacetyl imidazole (0.68 mL, 6.0 mmol) was added and the reaction was warmed to room temperature and stirred under a nitrogen atmosphere for 16 hours. At this time, 1N hydrochloric acid (300 mL) was added to the reaction followed by extraction with ether (350 mL). The organics were washed with brine (200 mL), dried over MgSO4 and concentrated in vacuo. The resulting yellow oil was used without further purification.

Workup

  1. temperaturethe reaction was warmed to room temperature
  2. stirringstirred under a nitrogen atmosphere for 16 hours
  3. extractionfollowed by extraction with ether (350 mL)
  4. washThe organics were washed with brine (200 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe resulting yellow oil was used without further purification

Sources & evidence

ORD record
ord-8369ff7ab4224ac68cfed2dc6fd54adf
Source dataset
uspto-grants-1997_09
Patent number
US05670532

Reaction notes

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