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Water → HCID 22591680, compound

HRID 1784495
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Reaction equation

HRID 1784495 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10]1[O:14][C:13]([C:15]23[CH2:22][CH2:21][C:18]([CH2:23][CH2:24][CH2:25][C:26](=[O:28])[CH3:27])([CH2:19][CH2:20]2)[CH2:17][CH2:16]3)=[N:12][N:11]=1.[BH4-].[Na+].C(OCC)(=O)C.O>CO>[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10]1[O:14][C:13]([C:15]23[CH2:22][CH2:21][C:18]([CH2:23][CH2:24][CH2:25][CH:26]([OH:28])[CH3:27])([CH2:19][CH2:20]2)[CH2:17][CH2:16]3)=[N:12][N:11]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 4311764Sodium borohydrideHCID 22591679HCID 22591679, compound

Product 1

HCID 22591680HCID 22591680, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

5-{4-[5-(2-Chloro-4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]bicyclo[2.2.2]oct-1-yl}pentan-2-one (5-H) (0.150 g, 0.373 mmol) was stirred in methanol (5 mL) at 0° C. Sodium borohydride (0.0169 g, 0.448 mmol) was added. The reaction was allowed to stir to room temperature. The mixture was then layered with ethyl acetate (20 mL) and water (20 mL). The ethyl acetate layer was extracted and dried (MgSO4). Solvent was removed in vacuo to afford 5-{4-[5-(2-chloro-4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]bicyclo[2.2.2]oct-1-yl}pentan-2-ol (5-I).

Workup

  1. extractionThe ethyl acetate layer was extracted
  2. dry with materialdried (MgSO4)
  3. customSolvent was removed in vacuo

Sources & evidence

ORD record
ord-d4d247fa61c34f7fb684e5173dbc37e3
Source dataset
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07504402B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes