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Depiction
Precursor
Dimethyl-[2-[4-[[(3,4,5-trimethoxybenzoyl)amino]methyl]phenoxy]ethyl]azanium
C[NH+](C)CCOC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C(=C2)OC)OC)OC
8 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
Trimethobenzamide N-Oxide
C[N+](C)(CCOC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C(=C2)OC)OC)OC)[O-]
Depth 1
Depiction
Product
Dimethyl-[2-[4-[[(3,4,5-trimethoxybenzoyl)amino]methyl]phenoxy]ethyl]azanium
C[NH+](C)CCOC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C(=C2)OC)OC)OC
Depiction
Precursor
Dimethyl-[2-[4-[[(3,4,5-trimethoxybenzoyl)amino]methyl]phenoxy]ethyl]azanium
C[NH+](C)CCOC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C(=C2)OC)OC)OC
Depth 3
Depiction
Downstream Successor
4-Hydroxybenzoic Acid
C(=O)(C1=CC=C(O)C=C1)O
Depiction
Precursor
Dimethyl-[2-[4-[[(3,4,5-trimethoxybenzoyl)amino]methyl]phenoxy]ethyl]azanium
C[NH+](C)CCOC1=CC=C(C=C1)CNC(=O)C2=CC(=C(C(=C2)OC)OC)OC
Depth 2
Depiction
Downstream Successor
4-Hydroxybenzyl Alcohol
OCC1=CC=C(C=C1)O
No Original Precursors

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