Water → HCID 59589532, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17]2[N:22]3[N:23]=[C:24]([NH:26][C:27]4[CH:32]=[CH:31][C:30]([O:33][CH2:34][CH2:35][N:36]5[CH2:40][CH2:39][CH2:38][CH2:37]5)=[CH:29][CH:28]=4)[N:25]=[C:21]3[CH:20]=[CH:19][CH:18]=2)[CH:12]=1)C.O>C(OCC)C>[N:36]1([CH2:35][CH2:34][O:33][C:30]2[CH:29]=[CH:28][C:27]([NH:26][C:24]3[N:25]=[C:21]4[CH:20]=[CH:19][CH:18]=[C:17]([C:13]5[CH:12]=[C:11]([CH2:10][OH:9])[CH:16]=[CH:15][CH:14]=5)[N:22]4[N:23]=3)=[CH:32][CH:31]=2)[CH2:40][CH2:39][CH2:38][CH2:37]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a slurry of lithium aluminium hydride (82.6 mg, 2.12 mmol) in diethylether (10 mL) was added 3-{2-[4-(2-pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzoic acid ethyl ester (0.50 g, 1.06 mmol) portionwise. The mixture was stirred at room temperature for 6 hrs. Water was added to quench the hydride and the aqueous layer was removed. The organic layer was concentrated in vacuo, and the crude product loaded onto an SCX column, which was washed with methanol and the product eluted with 2M ammonia in methanol, then concentrated in vacuo. Yield: 0.35 g, 76%. A small amount was purified by preparatory HPLC. RT: 2.32, MI: 430, Method: 2.
Workup
- customto quench the hydride
- customthe aqueous layer was removed
- concentrationThe organic layer was concentrated in vacuo
- washwas washed with methanol
- washthe product eluted with 2M ammonia in methanol
- concentrationconcentrated in vacuo
- customA small amount was purified by preparatory HPLC
- customRT
Sources & evidence
- ORD record
- ord-037a6934a5b84c79b952c4bc556830ba
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08431596B2
Reaction notes
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