Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1)

Base Information

Chemical Name:Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1)
CAS No.:77869-77-3
Molecular Formula:2C₂H₂O₄*C₁₉H₃₁N₃O
Molecular Weight:497.546
Hs Code.:
DSSTox Substance ID:DTXSID20228486
Mol file:77869-77-3.mol

Synonyms:77869-77-3;Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1);N-(2-(3-n-Butylhexahydropyrimidino)ethyl)propionanilide oxalate hydrate;DTXSID20228486;LS-119068

Suppliers and Price of Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1)

Supply Marketing:

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

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Chemical Property of Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1)

Chemical Property:

Vapor Pressure:9.81E-08mmHg at 25°C
Boiling Point:434°C at 760 mmHg
Flash Point:167.4°C
PSA：175.99000
LogP:1.38190
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:10
Exact Mass:497.23732970
Heavy Atom Count:35
Complexity:413

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN1CCCN(C1)CCN(C2=CC=CC=C2)C(=O)CC.C(=O)(C(=O)O)O.C(=O)(C(=O)O)O

Technology Process of Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1)

There total 4 articles about Propanamide, N-(2-(3-butyltetrahydro-1(2H)-pyrimidinyl)ethyl)-N-phenyl-, ethandioate, hydrate (2:4:1) 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: 21.1%

: 144-62-7,97993-78-7
oxalic acid

: 77869-76-2
N-<2-(3-n-butylhexahydropyrimidino)ethyl>propionanilide

: 77869-77-3
N-[2-(3-Butyl-tetrahydro-pyrimidin-1-yl)-ethyl]-N-phenyl-propionamide; compound with oxalic acid

Guidance literature:: In diethyl ether;
DOI:10.1248/cpb.28.3310

Reference yield:

: 1005-66-9
N-(β-bromoethyl)aniline hydrobromide

: 77869-77-3
N-[2-(3-Butyl-tetrahydro-pyrimidin-1-yl)-ethyl]-N-phenyl-propionamide; compound with oxalic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / ethanol / 4 h / Heating

2: benzene / 3 h / Heating

3: 21.1 percent / diethyl ether

In diethyl ether; ethanol; benzene;
DOI:10.1248/cpb.28.3310

Reference yield:

: 77869-64-8
N-<2-(3-n-butylhexahydropyrimidino)ethyl>aniline

: 77869-77-3
N-[2-(3-Butyl-tetrahydro-pyrimidin-1-yl)-ethyl]-N-phenyl-propionamide; compound with oxalic acid

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 3 h / Heating

2: 21.1 percent / diethyl ether

In diethyl ether; benzene;
DOI:10.1248/cpb.28.3310