Lithium Hydroxide → HCID 67847834, compound

HRID 231092Notes

Reaction equation

HRID 231092 reaction equation
C([O:8][C:9](=[O:39])[C@H:10]([CH2:30][C:31]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][CH:32]=1)[N:11]([C:20]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21])[C:12](=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])C1C=CC=CC=1.[Li+].[OH-]>O1CCCC1.O>[C:20]([N:11]([C:12](=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])[C@H:10]([C:9]([OH:39])=[O:8])[CH2:30][C:31]1[CH:36]=[CH:35][C:34]([O:37][CH3:38])=[CH:33][CH:32]=1)([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21]

Participants

5

Procedure

A solution of 2.66 g (5 mmol) of the resultant compound of Example 170 in 60 mL of tetrahydrofuran was cooled to 0° C., treated with 0.63 g (15 mmol) of LiOH in 30 mL of H2O and allowed to stir for 2 h. After concentration of the solvent, the mixture was partitioned between H2O and ether, acidified, extracted with ethyl acetate, dried over MgSO4 and concentrated to give 1.55 g (70%) of the desired compound.

Workup

  1. customAfter concentration of the solvent, the mixture was partitioned between H2O and ether
  2. extractionextracted with ethyl acetate
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-38353c8699c64e35925c49a08369e942
Source dataset
uspto-grants-1989_07
Patent number
US04845079

Reaction notes

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