HCID 54417295, compound → HCID 19851993, compound

HRID 1607150Notes

Reaction equation

HRID 1607150 reaction equation
C[O:2][C:3](=[O:33])[C:4]([NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][O:19][C:20]2[CH:25]=[CH:24][C:23]([C:26](=[O:28])[CH3:27])=[C:22]([OH:29])[C:21]=2[CH2:30][CH2:31][CH3:32])[CH:8]=1)=[O:5]>C1(C)C=CC=CC=1>[C:26]([C:23]1[CH:24]=[CH:25][C:20]([O:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][O:13][C:9]2[CH:8]=[C:7]([NH:6][C:4](=[O:5])[C:3]([OH:33])=[O:2])[CH:12]=[CH:11][CH:10]=2)=[C:21]([CH2:30][CH2:31][CH3:32])[C:22]=1[OH:29])(=[O:28])[CH3:27]

Participants

3

Reactant 1

HCID 54417295HCID 54417295, compound

Product 1

HCID 19851993HCID 19851993, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

starting from N-[3-(5-[4-acetyl-3-hydroxy-2-n-propylphenoxy]-pentyloxy)-phenyl]-oxamic acid methyl ester there is obtained N-{3-[5-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-pentyloxy]-phenyl}-oxamic acid having a melting point of 117°-118° (toluene) and the triethanolammonium salt thereof,

Sources & evidence

ORD record
ord-4dbaad59386a4aaca4057a99201bffd3
Source dataset
uspto-grants-1989_09
Patent number
US04863942

Reaction notes

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