2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-

Base Information

Chemical Name:2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-
CAS No.:101460-12-2
Molecular Formula:C₁₅H₁₈N₄
Molecular Weight:254.335
Hs Code.:
DSSTox Substance ID:DTXSID10358160
Wikidata:Q82138513
ChEMBL ID:CHEMBL1526767
Mol file:101460-12-2.mol

Synonyms:2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-;101460-12-2;CBMicro_044383;Oprea1_787986;MLS000061361;CHEMBL1526767;DTXSID10358160;HMS2320G18;ZINC00448984;AKOS000676424;SMR000070620;BIM-0044343.P001;4-phenyl-6-(1-piperidinyl)-2-pyrimidinamine

Suppliers and Price of 2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-

Supply Marketing:

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

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Chemical Property of 2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:254.153146591
Heavy Atom Count:19
Complexity:271

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCN(CC1)C2=NC(=NC(=C2)C3=CC=CC=C3)N

Technology Process of 2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)-

There total 4 articles about 2-Pyrimidinamine, 4-phenyl-6-(1-piperidinyl)- 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: 55.0%

: 506-93-4
guanidine nitrate

: 185245-65-2
3-methylthio-3-N-piperidino-1-phenyl-2-propen-1-one

: 101460-12-2
2-amino-4-N-piperidino-6-phenylpyrimidine

Guidance literature:: With sodium t-butanolate; In tert-butyl alcohol; for 20h; Heating;

Reference yield:

: 110-89-4
piperidine

: 101460-12-2
2-amino-4-N-piperidino-6-phenylpyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / ethanol / 7 h / Heating

2: 1) potassium carbonate / 1) acetone, reflux, 3 h, 2) r.t., 3 h

3: 55 percent / sodium t-butoxide / 2-methyl-propan-2-ol / 20 h / Heating

With potassium carbonate; sodium t-butanolate; In ethanol; tert-butyl alcohol;

Reference yield:

: 53354-69-1
benzoylthioacetic acid piperide

: 101460-12-2
2-amino-4-N-piperidino-6-phenylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 1) potassium carbonate / 1) acetone, reflux, 3 h, 2) r.t., 3 h

2: 55 percent / sodium t-butoxide / 2-methyl-propan-2-ol / 20 h / Heating

With potassium carbonate; sodium t-butanolate; In tert-butyl alcohol;