4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

Base Information

Chemical Name:4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide
CAS No.:212322-31-1
Molecular Formula:C₁₇H₁₈N₂O₃
Molecular Weight:298.342
Hs Code.:
DSSTox Substance ID:DTXSID801228324

Synonyms:SCHEMBL6776066;DUCVDUMTPPUUQT-UHFFFAOYSA-N;DTXSID801228324;212322-31-1;N-(4-Aminobenzoyl)-N-phenyl-I(2)-alanine methyl ester;4-Amino-benzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide;4-aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

Suppliers and Price of 4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:298.13174244
Heavy Atom Count:22
Complexity:372

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)CCN(C1=CC=CC=C1)C(=O)C2=CC=C(C=C2)N

Technology Process of 4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide

There total 2 articles about 4-Aminobenzoic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 212322-63-9
4-nitrobenzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide

: 212322-31-1
4-aminobenzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; for 3h; under 2250.23 Torr;

Reference yield:

: 21911-84-2
methyl 3-(phenylamino)propanoate

: 212322-31-1
4-aminobenzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / N,N-dimethyl-formamide / 1 h / Reflux

1.2: 1 h / 20 °C

2.1: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 2250.23 Torr

With thionyl chloride; palladium 10% on activated carbon; hydrogen; In methanol; N,N-dimethyl-formamide;

Reference yield: 69.0%

: 212322-31-1
4-aminobenzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide

: 4435-44-3
2-thioxobutane

: C₂₁H₂₂N₂O₃S

Guidance literature:: 4-aminobenzoic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide; With tert-butylhypochlorite; In dichloromethane; at -70 ℃; for 2h;

2-thioxobutane; In dichloromethane; at -78 - 20 ℃;