Water → HCID 85860577, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]2[CH2:7][CH:6]([C:11](O)=[O:12])[CH2:5][C:4]=2[N:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]2[CH2:7][CH:6]([CH2:11][OH:12])[CH2:5][C:4]=2[N:3]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1.83 g (9.26 mmol) of (+/−)2-chloro-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid (prepared by analogy to the method described in WO 99/02517) in 50 ml of anhydrous tetrahydrofuran under argon was added 0.52 g (13.89 mmol) of lithium aluminum hydride. The resulting mixture was stirred at room temperature for 2 h. Excess of lithium aluminum hydride was hydrolyzed with 2.13 ml of water and 0.53 ml of sodium hydroxide (15%). The precipitate was filtered off and washed with diethyl ether, the filtrate was evaporated to give 1.61 g (95%) of product as an oil.
Workup
- filtrationThe precipitate was filtered off
- washwashed with diethyl ether
- customthe filtrate was evaporated
Sources & evidence
- ORD record
- ord-fe72bcccaa174a29a0a7714d71450460
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07465737B2
Reaction notes
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