Reaction equation
[ClH:1].Cl.[NH2:3][C@@H:4]([CH2:13][CH3:14])[C@H:5]([OH:12])[C:6]([NH:8][CH:9]1[CH2:11][CH2:10]1)=[O:7].[N+](CCCC)#[C-:16]>>[ClH:1].[ClH:1].[NH2:3][C@@H:4]([CH2:13][CH3:14])[C@H:5]([OH:12])[C:6]([NH:8][CH2:9][CH2:11][CH2:10][CH3:16])=[O:7]Participants
3
Procedure
The title compound was prepared in analogy to (2S,3S)-3-amino-N-cyclopropyl-2-hydroxypentanamide dihydrochloride, Representative Procedure A, using 1-isocyanobutane in the third step (A3).
Sources & evidence
- ORD record
- ord-551a472e17a14fffa215e687d2150b68
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08729061B2
Linked notes
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