Acetate → Isopropyl 2-(3-(6-ethyl-1-naphthamido)phenoxy)acetate

HRID 472785Notes

Reaction equation

HRID 472785 reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([C:13]([OH:15])=O)=[CH:8][CH:7]=[CH:6]2)[CH3:2].[NH2:16][C:17]1[CH:18]=[C:19]([CH:28]=[CH:29][CH:30]=1)[O:20][CH2:21][C:22]([O:24][CH:25]([CH3:27])[CH3:26])=[O:23].C([O-])(=O)C>>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([C:13]([NH:16][C:17]1[CH:18]=[C:19]([CH:28]=[CH:29][CH:30]=1)[O:20][CH2:21][C:22]([O:24][CH:25]([CH3:26])[CH3:27])=[O:23])=[O:15])=[CH:8][CH:7]=[CH:6]2)[CH3:2]

Participants

4

Reactant 3

HCID 175AcetateHCID 10608474Isopropyl 2-(3-aminophenoxy)acetateHCID 666608456-Ethyl-1-naphthoic acid

Product 1

HCID 86762264Isopropyl 2-(3-(6-ethyl-1-naphthamido)phenoxy)acetate

Procedure

In accordance with the procedure of Example 1, step 5, 6-ethyl-1-naphthoic acid (51 mg, 0.25 mmol) and isopropyl 2-(3-aminophenoxy)acetate (64 mg, 0.31 mmol) were converted into 34 mg (34%) of isopropyl 243-(6-ethyl-1-naphthamido)phenoxy)acetate.

Sources & evidence

ORD record
ord-112e19a4627f400a86a8dd8a1d07bbc2
Source dataset
uspto-grants-2014_01
Patent number
US08633220B2

Reaction notes

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