HCID 18794828, compound → HCID 18794843, compound

HRID 400121Notes

Reaction equation

HRID 400121 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]([O: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]>CO>[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]([O: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 18794828HCID 18794828, compound

Product 1

HCID 18794843HCID 18794843, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The title compound, mp 164°-5° C. (methanol), was prepared from methyl 3-[4-[2-[N-(2-benzoxazolyl)-N-methylamino]ethoxy]phenyl]-2-(4-chlorophenoxy)propanoate by a procedure analogous to that described in Example 2.

Sources & evidence

ORD record
ord-bd33b75c67954b40bd4399265b9a7e41
Source dataset
uspto-grants-1998_10
Patent number
US05827865

Reaction notes

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