5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

Base Information

Chemical Name:5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile
CAS No.:116615-95-3
Molecular Formula:C₁₇H₁₉N₃OS
Molecular Weight:313.423
Hs Code.:

Synonyms:5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

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Chemical Property of 5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

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Technology Process of 5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

There total 8 articles about 5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile 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:

: 116615-89-5
(R)-3-Benzyl-5-mercaptomethyl-imidazolidine-2,4-dione

: 116615-95-3
5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / CH₂Cl₂ / 1 h / 23 °C

2: 85 percent / BuLi, cerium trichloride / tetrahydrofuran / 0.5 h / -78 °C

3: 94 percent / diisobutylaluminium hydride / toluene / 1 h / -78 °C

4: 69 percent / tri-n-butylphosphine / CH₂Cl₂ / 3 h / 23 °C

5: tricyclohexyltin hydride, AIBN / benzene / 2 h / Heating

6: aq. ethanol / 10 h / Heating

With n-butyllithium; cerium(III) chloride; tricyclohexyltin hydride; 2,2'-azobis(isobutyronitrile); tributylphosphine; diisobutylaluminium hydride; In tetrahydrofuran; ethanol; dichloromethane; toluene; benzene;
DOI:10.1016/0040-4039(88)80015-7

Reference yield:

: 116615-88-4
(R)-2-(3-Benzyl-ureido)-3-mercapto-propionic acid methyl ester

: 116615-95-3
5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

Guidance literature:: Multi-step reaction with 7 steps

1: 91 percent / 6 N HCl / 45 h / 100 °C

2: 89 percent / CH₂Cl₂ / 1 h / 23 °C

3: 85 percent / BuLi, cerium trichloride / tetrahydrofuran / 0.5 h / -78 °C

4: 94 percent / diisobutylaluminium hydride / toluene / 1 h / -78 °C

5: 69 percent / tri-n-butylphosphine / CH₂Cl₂ / 3 h / 23 °C

6: tricyclohexyltin hydride, AIBN / benzene / 2 h / Heating

7: aq. ethanol / 10 h / Heating

With hydrogenchloride; n-butyllithium; cerium(III) chloride; tricyclohexyltin hydride; 2,2'-azobis(isobutyronitrile); tributylphosphine; diisobutylaluminium hydride; In tetrahydrofuran; ethanol; dichloromethane; toluene; benzene;
DOI:10.1016/0040-4039(88)80015-7

Reference yield:

: 116615-92-0
(4R,5R)-1-Benzyl-4-(5-chloro-pent-1-ynylsulfanylmethyl)-5-hydroxy-imidazolidin-2-one

: 116615-95-3
5-[(3aR,6aS)-1-Benzyl-2-oxo-hexahydro-thieno[3,4-d]imidazol-(6E)-ylidene]-pentanenitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / tri-n-butylphosphine / CH₂Cl₂ / 3 h / 23 °C

2: tricyclohexyltin hydride, AIBN / benzene / 2 h / Heating

3: aq. ethanol / 10 h / Heating

With tricyclohexyltin hydride; 2,2'-azobis(isobutyronitrile); tributylphosphine; In ethanol; dichloromethane; benzene;
DOI:10.1016/0040-4039(88)80015-7