Sodium Hydroxide → HCID 50992301, compound
Reaction equation
[C:1]1([CH:7]2[CH2:12][CH2:11][N:10]([C:13]3[C:22]([N:23]4[CH2:28][CH2:27][CH:26]([C:29]5[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=5)[CH2:25][CH2:24]4)=[N:21][C:20]4[C:15](=[CH:16][CH:17]=[C:18]([C:35]([O:37]CC)=[O:36])[CH:19]=4)[N:14]=3)[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>CO.O>[C:1]1([CH:7]2[CH2:8][CH2:9][N:10]([C:13]3[C:22]([N:23]4[CH2:24][CH2:25][CH:26]([C:29]5[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=5)[CH2:27][CH2:28]4)=[N:21][C:20]4[C:15](=[CH:16][CH:17]=[C:18]([C:35]([OH:37])=[O:36])[CH:19]=4)[N:14]=3)[CH2:11][CH2:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 50 °C
Procedure
Into a 50-mL round-bottom flask, was placed a solution of ethyl 2,3-bis(4-phenylpiperidin-1-yl)quinoxaline-6-carboxylate (150 mg, 0.29 mmol, 1.00 equiv) in methanol (25 mL) and a solution of sodium hydroxide (58 mg, 1.45 mmol, 5.00 equiv) in water (2 mL). The resulting solution was stirred for 3 h at 50° C. in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 30 mL of water. The pH value of the aqueous solution was adjusted to 3 with 1N hydrochloric acid. The resulting solids were collected by filtration. The solid was dried in an oven under reduced pressure and purified by re-crystallization from methanol. This resulted in 80 mg (56%) of 2,3-bis(4-phenylpiperidin-1-yl)quinoxaline-6-carboxylic acid as a yellow solid.
Workup
- customInto a 50-mL round-bottom flask, was placed
- concentrationThe resulting mixture was concentrated under vacuum
- additionThe resulting solution was diluted with 30 mL of water
- filtrationThe resulting solids were collected by filtration
- customThe solid was dried in an oven under reduced pressure
- custompurified by re-crystallization from methanol
- customThis resulted in 80 mg (56%) of 2,3-bis(4-phenylpiperidin-1-yl)quinoxaline-6-carboxylic acid as a yellow solid
Sources & evidence
- ORD record
- ord-4b67f84ce8314a9c99735f1c0f464edd
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09193693B2
Reaction notes
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