Reaction #1269844
ord-eabe886922f44740a0e2dee11993f525
Reaction equation
diethyl azodicarboxylate
2-((1R,2R)-2-hydroxycyclopentylamino)-3-methylpyrimidin-4(3H)-one
triphenylphosphine
→
product
Yield 92.0%
(3aS,8aR)-7-Methyl-1,2,3,3a,7,8a-hexahydro-3b,7,8-triaza-cyclopenta[a]inden-6-one
Yield 92.0%
Reactants
Reagents
None
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherSolvent is removed under vacuum
- 2workup.ADDITIONthe residue is treated with 0.02 N HCl (40 mL)
- 3FiltrationThe precipitate is filtered off
- 4Washthe filtrate is washed with CH2Cl2
- 5OtherThe aqueous phase is evaporated to dryness under high vacuum
Procedure
To a solution of 2-((1R,2R)-2-hydroxycyclopentylamino)-3-methylpyrimidin-4(3H)-one (130 mg, 0.62 mmol) in anhydrous THF (2 mL) is added triphenylphosphine (163 mg, 0.62 mmol). Five minutes later, diethyl azodicarboxylate (DEAD, 0.45 mL, 0.93 mmol) in toluene is added dropwise. The mixture is stirred at room temperature for 2 hours. Solvent is removed under vacuum, the residue is treated with 0.02 N HCl (40 mL). The precipitate is filtered off, and the filtrate is washed with CH2Cl2. The aqueous phase is evaporated to dryness under high vacuum to give product as solids (108 mg, yield 92%), which is used for the next reaction without further purification. MS (ESI) m/z 192.1 [M+H]+.