Lithium Hydroxide → HCID 12148809, compound

HRID 1394830Notes

Reaction equation

HRID 1394830 reaction equation
C[O:2][C:3]([C:5]1[O:6][C:7]2[CH:13]=[CH:12][C:11]([NH:14][C:15]([C:17]3[C:18]([C:23]4[CH:28]=[CH:27][C:26]([C:29]([F:32])([F:31])[F:30])=[CH:25][CH:24]=4)=[CH:19][CH:20]=[CH:21][CH:22]=3)=[O:16])=[CH:10][C:8]=2[CH:9]=1)=[O:4].[Li+].[OH-]>C1COCC1.CO.O>[F:32][C:29]([F:30])([F:31])[C:26]1[CH:25]=[CH:24][C:23]([C:18]2[C:17]([C:15]([NH:14][C:11]3[CH:12]=[CH:13][C:7]4[O:6][C:5]([C:3]([OH:4])=[O:2])=[CH:9][C:8]=4[CH:10]=3)=[O:16])=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:28][CH:27]=1

Participants

6

Procedure

The product from step (c) (8.1 g) was dissolved in THF (100 mL) and methanol (100 mL). Under stirring conditions was added LiOH (2 g) in water (100 mL). The reaction mixture was stirred at room temperature for 30 minutes. The reaction solution was then concentrated in vacuo, acidified by adding 1N HCl solution. The product was extracted with ether (2×300 mL), and combined organic layers were washed with brine (2×50 mL) and then dried over MgSO4. The organic layer was then concentrated in vacuo to give the crude product which was purified by recrystallization from ether/hexane to give 7.1 g of the title compound.

Workup

  1. concentrationThe reaction solution was then concentrated in vacuo
  2. additionby adding 1N HCl solution
  3. extractionThe product was extracted with ether (2×300 mL)
  4. washwere washed with brine (2×50 mL)
  5. dry with materialdried over MgSO4
  6. concentrationThe organic layer was then concentrated in vacuo
  7. customto give the crude product which
  8. customwas purified by recrystallization from ether/hexane

Sources & evidence

ORD record
ord-d7799009d0db4d4999ea1cb92e09284b
Source dataset
uspto-grants-2008_03
Patent number
US07348355B2

Reaction notes

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