8-Pyrrolidinyl-5,6,7,8-tetrahydroquinoline → (+/-)-Decahydro-8-(-pyrrolidinyl)-quinoline
Reaction equation
[N:1]1([CH:6]2[C:15]3[N:14]=[CH:13][CH:12]=[CH:11][C:10]=3[CH2:9][CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.C(O)C.[Na]>>[N:1]1([CH:6]2[CH:15]3[CH:10]([CH2:11][CH2:12][CH2:13][NH:14]3)[CH2:9][CH2:8][CH2:7]2)[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
3
Procedure
This product is obtained mixed with other diastereoisomers by reduction of the product obtained in Step B either by catalytic hydrogenation or by a sodium-ethanol mixture. The description of these two reductions is given at the end of Example 4.
Workup
- customThis product is obtained
Sources & evidence
- ORD record
- ord-d2c435a4917c4e43ab3aa6bab1e494df
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04968700
Reaction notes
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