2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-

Base Information

Chemical Name:2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-
CAS No.:188299-19-6
Molecular Formula:C17H18N2O
Molecular Weight:266.343
Hs Code.:
DSSTox Substance ID:DTXSID20459177
Nikkaji Number:J1.590.537I
Wikidata:Q82282849

Synonyms:188299-19-6;2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-;SCHEMBL2733147;DTXSID20459177;1,3-Dimethyl-4beta,5alpha-diphenylimidazolidine-2-one

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Supply Marketing:

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

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Chemical Property of 2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:266.141913202
Heavy Atom Count:20
Complexity:313

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1C(C(N(C1=O)C)C2=CC=CC=C2)C3=CC=CC=C3
Isomeric SMILES:CN1[C@H]([C@@H](N(C1=O)C)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-

There total 9 articles about 2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)- 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: 48.0%

: 2579-22-8
Phenylpropargyl aldehyde

: Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide

: t-butyl (2S,3S)-1-benzyl-3-phenylethynylaziridine-2-carboxylate

: t-butyl (2R,3R)-1-benzyl-3-phenylethynylaziridine-2-carboxylate

: t-butyl (2R,3S)-1-benzyl-3-phenylethynylaziridine-2-carboxylate

: 188299-19-6
(S,S)-1,3-dimethyl-4,5-diphenylimidazolidin-2-one

Guidance literature:: Phenylpropargyl aldehyde; Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide; With N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; at 25 ℃; for 72h;

With acetic anhydride; In tetrahydrofuran; chloroform; at 20 ℃; for 0.5h;
DOI:10.1021/jo051495j

Reference yield: 41.0%

: 3163-37-9,51534-41-9,22644-96-8
(E)-hexadec-2-enal

: Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide

: t-butyl (2S,3S)-1-benzyl-3-(pentadec-1-enyl)aziridine-2-carboxylate

: 871259-09-5
t-butyl (2R,3S)-1-benzyl-3-(pentadec-1-enyl)aziridine-2-carboxylate

: 871259-08-4
t-butyl (2R,3R)-1-benzyl-3-(pentadec-1-enyl)aziridine-2-carboxylate

: 188299-19-6
(S,S)-1,3-dimethyl-4,5-diphenylimidazolidin-2-one

Guidance literature:: (E)-hexadec-2-enal; Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide; With N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; at 25 ℃; for 72h;

With silica gel; In tetrahydrofuran; chloroform; at 20 ℃; for 72h; Title compound not separated from byproducts;
DOI:10.1021/jo051495j

Reference yield: 33.0%

: 1192-88-7
1-cyclohexene-1-carboxaldehyde

: Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide

: t-butyl (2R,3S)-1-benzyl-3-(cyclohex-1-en-1-yl)aziridine-2-carboxylate

: t-butyl (2R,3R)-1-benzyl-3-(cyclohex-1-en-1-yl)aziridine-2-carboxylate

: 188299-19-6
(S,S)-1,3-dimethyl-4,5-diphenylimidazolidin-2-one

Guidance literature:: 1-cyclohexene-1-carboxaldehyde; Benzyl-tert-butoxycarbonylmethyl-((4S,5S)-1,3-dimethyl-4,5-diphenyl-imidazolidin-2-ylidene)-ammonium; bromide; With N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; at 25 ℃; for 72h;

With silica gel; In tetrahydrofuran; chloroform; at 20 ℃; for 72h;
DOI:10.1021/jo051495j