Acetic Acid → HCID 14180887, compound
Reaction equation
[ClH:1].C[CH2:3][CH2:4][CH2:5][C@H:6]([NH:15]C(=O)OC(C)(C)C)[C:7](=[O:14])[CH2:8][NH:9][CH2:10][CH:11]([CH3:13])[CH3:12].[C:23](O)(=O)C>Cl>[ClH:1].[ClH:1].[NH2:15][C@@H:6]([CH2:5][CH:4]([CH3:3])[CH3:23])[C:7](=[O:14])[CH2:8][NH:9][CH2:10][CH:11]([CH3:12])[CH3:13]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(S)-[4-Methyl-1-[[(2-methylpropyl)amino]acetyl]butyl]carbamic acid, 1,1-dimethylethyl ester, hydrochloride (0.66 g, 1.95 mmol) was dissolved in a solution of hydrogen chloride in acetic acid (1.5N, 7 ml) and allowed to stand at room temperature for 20 minutes. It was evaporated in vacuo and then re-evaporated from benzene. The residue was crystallized from isopropanol yielding 240 mg of the title compound, melting point 148°-150° C.
Workup
- customIt was evaporated in vacuo
- customre-evaporated from benzene
- customThe residue was crystallized from isopropanol yielding 240 mg of the title compound, melting point 148°-150° C.
Sources & evidence
- ORD record
- ord-388e42087ba84329b2f18b3f671ca3c0
- Source dataset
- uspto-grants-1988_06
- Patent number
- US04749792
Reaction notes
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