Aluminium lithium hydride → HCID 178477845, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[C:16]3[CH2:21][CH2:20][N:19]([C:22](=O)[CH2:23][CH2:24][C:25]4[N:26]=[CH:27][NH:28][CH:29]=4)[CH2:18][CH2:17]3)[C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[CH2:8][CH2:7][C:6]=2[CH:31]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1.C(OCC)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[C:16]3[CH2:21][CH2:20][N:19]([CH2:22][CH2:23][CH2:24][C:25]4[N:26]=[CH:27][NH:28][CH:29]=4)[CH2:18][CH2:17]3)[C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[CH2:8][CH2:7][C:6]=2[CH:31]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of compound (16) (0.65 g; 1.5 mmol) in anhydrous tetrahydrofuran (70 ml) was added a 1.0M solution of lithium aluminum hydride in tetrahydrofuran (4.6 ml; 4.6 mmol). The mixture was stirred at room temperature for 1.75 h. then diluted with ethyl ether and quenched with dropwise addition of saturated ammonium chloride solution. To saturated ammonium chloride
Workup
- customquenched with dropwise addition of saturated ammonium chloride solution
Sources & evidence
- ORD record
- ord-22358971c83f4092b5329af7a85fcbbb
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506756B2
Reaction notes
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