Lithium Hydroxide → HCID 67076738, compound

HRID 2094676Notes

Reaction equation

HRID 2094676 reaction equation
C[O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[C:6]([O:12][CH2:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]#[N:22])[CH:16]=2)[CH:5]=1.[OH-].[Li+]>O1CCOCC1>[C:21]([C:17]1[CH:16]=[C:15]([CH2:14][CH2:13][O:12][C:6]2[CH:5]=[C:4]([CH:9]=[CH:8][C:7]=2[O:10][CH3:11])[C:3]([OH:23])=[O:2])[CH:20]=[CH:19][CH:18]=1)#[N:22]

Participants

4

Conditions

Temperature
60 °C

Procedure

The compound of step 2 (274 mg, 0.883 mmol) was dissolved in dioxane (4.5 ml), lithium hydroxide (4.42 ml of a 1 M aqueous solution, 4.42 mmol) was added, and the mixture was stirred at 60° C. for 30 min. The mixture was partitioned between 2 N hydrochloric acid and EA, the aqueous phase extracted with EA, and the combined organic extracts were dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by preparative RP HPLC (water/ACN gradient) to give 160 mg of the title compound.

Workup

  1. customThe mixture was partitioned between 2 N hydrochloric acid and EA
  2. extractionthe aqueous phase extracted with EA
  3. dry with materialthe combined organic extracts were dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated to dryness
  6. customThe residue was purified by preparative RP HPLC (water/ACN gradient)

Sources & evidence

ORD record
ord-1230a39a3ee8495fba1a5bc14f8e6a78
Source dataset
uspto-grants-2013_05
Patent number
US08445530B2

Reaction notes

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