Triethylamine → (R)-N5-(Cbz)-N2-(Diphenylacetyl)-(R)-N-(2-hydroxy-1-phenylethyl)-ornithine amide
Reaction equation
Cl.[C:2]([NH:12][CH2:13][CH2:14][CH2:15][C@H:16]([C:18]([NH:20][C@H:21]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[CH2:22][OH:23])=[O:19])[NH2:17])([O:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:3].C(N([CH2:35][CH3:36])CC)C>C(Cl)Cl>[C:2]([NH:12][CH2:13][CH2:14][CH2:15][C@H:16]([C:18]([NH:20][C@H:21]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)[CH2:22][OH:23])=[O:19])[NH:17][C:22](=[O:23])[CH:21]([C:36]1[CH:35]=[CH:5][CH:6]=[CH:7][CH:8]=1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)([O:4][CH2:5][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)=[O:3]Participants
4
Procedure
Prepared according to the method described in Example 1(d) above from (R)-N5 -(Cbz)-(R)-N-(2-hydroxy-1-phenylethyl)ornithine amide hydrochloride (2.6 g; 6.16 mmol; from step (b) above), 2-nitrophenyl diphenyl acetate (2.37 g; 7.39 mmol; see Example 1(c) above) and triethylamine (1.28 mL; 9.24 mmol) in 150 mL of CH2Cl2, yielding 2.5 g of the sub-title compound as a white, crystalline material.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-3b7ef6b26a52445ebfe39fc0c0b513f5
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06127414
Reaction notes
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