(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

Base Information

Chemical Name:(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea
CAS No.:1314406-19-3
Molecular Formula:C₂₁H₂₂N₄O₂S
Molecular Weight:394.497
Hs Code.:

Synonyms:(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

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Chemical Property of (RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

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Technology Process of (RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

There total 6 articles about (RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea 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: 75.0%

: 927970-47-6
(RS)-6-acetamido-4-amino-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran

: 2719-32-6
4-isothiocyanatobenzonitrile

: 1314406-19-3
(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

Guidance literature:: In dichloromethane; for 0.5h;
DOI:10.1016/j.bmc.2011.05.040

Reference yield:

: 186774-68-5
C₁₃H₁₆N₂O₃

: 1314406-19-3
(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / methanol / 3750.38 Torr

2: dichloromethane / 0.5 h

With hydrogen; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2011.05.040

Reference yield:

: 7298-67-1
5-acetamido-2-hydroxyacetophenone

: 1314406-19-3
(RS)-N-4-cyanophenyl-N'-(6-acetamido-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)thiourea

Guidance literature:: Multi-step reaction with 4 steps

1: pyrrolidine / methanol / 25 °C

2: hydroxylamine hydrochloride; potassium carbonate / ethanol / 3 h / Reflux

3: hydrogen / methanol / 3750.38 Torr

4: dichloromethane / 0.5 h

With pyrrolidine; hydroxylamine hydrochloride; hydrogen; potassium carbonate; In methanol; ethanol; dichloromethane;
DOI:10.1016/j.bmc.2011.05.040