Reaction #1869182
ord-36a25b36fc474b1286cb28173d92e0f6
Reaction equation
trisamine
compound
4-benzyl-3,4-dihydro-5H-spiro[1,4-benzoxazepine-2,4′-piperidin]-5-one
cyclopentanecarbonylchloride
→
4-benzyl-1′-(cyclopentylcarbonyl)-3,4-dihydro-5H-spiro[1,4-benzoxazepine-2,4′-piperidin]-5-one
Reactants
Reagents
None
Solvents
Conditions
Temperature
25°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1workup.STIRRINGthe mixture was stirred overnight at 25° C
- 2FiltrationThe mixture was filtered
- 3Concentrationthe filtrate was concentrated
- 4Otherto give the compound of the present invention
Procedure
To a solution of the compound prepared in Example 30 (0.010 mmol) in dichloroethane (0.7 mL) were added cyclopentanecarbonylchloride (0.020 mmol) and poly(4-vinylpyridine) (2% cross-linked, Aldrich, CAS#9017-40-7) (5.3 mg). The mixture was stirred overnight at 25° C. To the reaction mixture was added PS-trisamine (Argonaut, product number 800229, loading; 4.36 mmol/g) (6.9 mg), and the mixture was stirred overnight at 25° C. The mixture was filtered and the filtrate was concentrated to give the compound of the present invention having the following physical data.