Sodium Hydroxide → HCID 18461100, compound
Reaction equation
C(OC([N:6]1[CH:11]2[CH:12]([O:14]C3CCCCO3)[CH2:13][CH:7]1[CH2:8][CH:9]([CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH2:10]2)=O)C.C[Si](I)(C)C.[OH-].[Na+].S([O-])([O-])=O.[Na+].[Na+]>C(Cl)(Cl)Cl>[CH2:21]([CH:9]1[CH2:10][CH:11]2[NH:6][CH:7]([CH2:13][CH:12]2[OH:14])[CH2:8]1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the 3-benzyl-6-(tetrahydro-pyran-2-yloxy)-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid ethyl ester and 0.5 mL of trimethylsilyl iodide in 25 mL of chloroform was kept at room temperature for 48 h, shaken with 25 mL of 6N NaOH and dilute sodium sulfite and dried over magnesium sulfate. Removal of solvents gave 0.2 g of a resin.
Workup
- dry with materialdried over magnesium sulfate
- customRemoval of solvents
Sources & evidence
- ORD record
- ord-938313be508d4345beaefbe01d0dc735
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06432976B1
Reaction notes
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