HCID 23362231, compound → HCID 23362238, compound

HRID 1082121Notes

Reaction equation

HRID 1082121 reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[N:10]([CH2:12][CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH:22]([S:27][C:28]2[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][CH:29]=2)[C:23]([O:25]C)=[O:24])=[CH:17][CH:16]=1)[CH3:11]>C1(C)C=CC=CC=1>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[N:10]([CH2:12][CH2:13][O:14][C:15]1[CH:16]=[CH:17][C:18]([CH2:21][CH:22]([S:27][C:28]2[CH:29]=[CH:30][C:31]([Cl:34])=[CH:32][CH:33]=2)[C:23]([OH:25])=[O:24])=[CH:19][CH:20]=1)[CH3:11]

Participants

3

Reactant 1

HCID 23362231HCID 23362231, compound

Product 1

HCID 23362238HCID 23362238, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

The title compound, mp 156.1°-157.4° C. (toluene), was prepared from methyl 3-[4-[2-[N-(2-benzoxazolyl)-N-methylamino)ethoxy]phenyl]-2-(4-chlorophenylthio)propanoate by a procedure similar to that described in Example 24.

Sources & evidence

ORD record
ord-7d9a193bbb9e4611bca7742e91601e27
Source dataset
uspto-grants-1996_12
Patent number
US05589492

Reaction notes

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