HCID 11107379, compound → HCID 54189462, compound

HRID 1457830Notes

Reaction equation

HRID 1457830 reaction equation
[C:1]([O:4][CH2:5][C@@H:6]([C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:7][O:8]C(=O)C)(=[O:3])[NH2:2].C(OC[C@@H](C1C=CC=CC=1)COC(=O)C)(=O)N>>[C:1]([O:4][CH2:5][C@@H:6]([C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[CH2:7][OH:8])(=[O:3])[NH2:2]

Participants

3

Reactant 2

HCID 11107379HCID 11107379, compoundHCID 67572415HCID 67572415, compound

Product 1

HCID 54189462HCID 54189462, compoundYield 78.9%

Procedure

The title compound was synthesized in a similar manner to that of Example XXII, except that (S)-3-acetoxy-2-(2,4-dichlorophenyl)propanol carbamate, instead of (S)-3-acetoxy-2-phenylpropanol carbamate, was used as a starting material. Yield 78.9%. Purity 99.7%.

Sources & evidence

ORD record
ord-8084361cde634a0091169c7baa442084
Source dataset
uspto-grants-1998_12
Patent number
US05849772

Reaction notes

Loading…