1-Piperazinecarboxylic acid, ethyl ester → 1-(Oxan-4-yl)piperazine
Reaction equation
C(O[C:4]([N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=O)C.[O:12]1[CH2:17][CH2:16]C(=O)[CH2:14][CH2:13]1>>[O:12]1[CH2:17][CH2:16][CH:4]([N:6]2[CH2:7][CH2:8][NH:9][CH2:10][CH2:11]2)[CH2:14][CH2:13]1Participants
3
Procedure
By the reaction and treatment in the same manner as in Starting Material Synthetic Example 10 using 1-ethoxycarbonylpiperazine (50 g) and 2,3,5,6-tetrahydropyran-4-one (34 g), the title compound (21 g) was obtained. boiling point: 95-100° C./5 mmHg
Workup
- customBy the reaction and treatment in the same manner as
Sources & evidence
- ORD record
- ord-fd2ef17b5cfd485a8d92e094603fa3c0
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07112594B2
Reaction notes
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