HCID 23362243, compound → HCID 23362233, compound

HRID 1082112Notes

Reaction equation

HRID 1082112 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]([F:28])[C:23]([O:25]CC)=[O:24])=[CH:17][CH:16]=1)[CH3:11]>ClCCl>[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]([F:28])[C:23]([OH:25])=[O:24])=[CH:17][CH:16]=1)[CH3:11]

Participants

3

Reactant 1

HCID 23362243HCID 23362243, compound

Product 1

HCID 23362233HCID 23362233, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The title compound, mp 146°-8° C. (dichloromethane) was prepared from ethyl 3-[4-[2-[N-(2-benzoxazolyl)-N-methylamino]ethoxy]phenyl]-2-fluoropropanoate by a procedure similar to that described for Example 6.

Sources & evidence

ORD record
ord-7b9b6036169642d78e3398d30ddfc252
Source dataset
uspto-grants-1996_12
Patent number
US05589492

Reaction notes

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