Aluminium lithium hydride → HCID 89874839, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[C:7]([CH3:18])=[CH:8][C:9]([C:12](N(OC)C)=[O:13])=[N:10][CH:11]=2)[CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>>[CH:1]1([CH2:4][O:5][C:6]2[C:7]([CH3:18])=[CH:8][C:9]([CH:12]=[O:13])=[N:10][CH:11]=2)[CH2:2][CH2:3]1Participants
3
Procedure
The title compound is prepared in >99% yield (495 mg, pale orange solid) from 5-(cyclopropylmethoxy)-N-methoxy-N,4-dimethylpicolinamide (622 mg, 2.49 mmol, Step-4) and lithium aluminum hydride (47 mg, 1.2 mmol) in a similar manner to Step-2 of Amine-3.
Sources & evidence
- ORD record
- ord-89b6c53ecc924a2383c73d7a034d7e6d
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187475B2
Reaction notes
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