HCID 53875108, compound → HCID 19851986, compound

HRID 1607149Notes

Reaction equation

HRID 1607149 reaction equation
C[O:2][C:3](=[O:32])[C:4]([NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH2:15][CH2:16][O:17][C:18]2[CH:23]=[CH:22][C:21]([C:24](=[O:26])[CH3:25])=[C:20]([OH:27])[C:19]=2[CH2:28][CH2:29][CH3:30])[C:8]=1[CH3:31])=[O:5]>C1(C)C=CC=CC=1>[C:24]([C:21]1[CH:22]=[CH:23][C:18]([O:17][CH2:16][CH2:15][CH2:14][O:13][C:9]2[C:8]([CH3:31])=[C:7]([NH:6][C:4](=[O:5])[C:3]([OH:32])=[O:2])[CH:12]=[CH:11][CH:10]=2)=[C:19]([CH2:28][CH2:29][CH3:30])[C:20]=1[OH:27])(=[O:26])[CH3:25]

Participants

3

Procedure

In analogous manner, starting from N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-2-methylphenyl}-oxamic acid methyl ester there is obtained N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-2-methylphenyl}-oxamic acid having a melting point of 146°-148° (toluene) and the triethanolammonium salt thereof having a melting point of 114°-115°,

Sources & evidence

ORD record
ord-c00d940fe0c344c792f758c8215c5e39
Source dataset
uspto-grants-1989_09
Patent number
US04863942

Reaction notes

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