4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

Base Information

Chemical Name:4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide
CAS No.:294644-47-6
Molecular Formula:C₂₁H₁₈ClN₃Se
Molecular Weight:426.807
Hs Code.:

4-chloro-N<sup>1</sup>-{[(methyl)(phenyl)amino](selenocarbonyl)}-N<sup>2</sup>-phenylbenzimidamide

Synonyms:4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

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Chemical Property of 4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

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Technology Process of 4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

There total 2 articles about 4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide 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: 92.0%

: 100-61-8
N-methylaniline

: 4-chloro-N-phenylbenzimidoyl isoselenocyanate

: 294644-47-6
4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

Guidance literature:: In acetone; at 25 ℃;
DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M

Reference yield:

: 6833-15-4
4-chlorobenzanilide

: 294644-47-6
4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / 3 h / Heating

2: acetone

3: 92 percent / acetone / 25 °C

With thionyl chloride; In acetone; 1: Substitution / 2: Substitution / 3: Addition;
DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M

Reference yield:

: 294644-47-6
4-chloro-N¹-{[(methyl)(phenyl)amino](selenocarbonyl)}-N²-phenylbenzimidamide

: 4-(4-chlorophenyl)-N-methyl-N-phenyl-1,3-selenazol-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1: acetone / 25 °C

2: Et₃N / acetone

3: 76 percent / NaOH; H₂O / acetone / 2 h / Heating

With sodium hydroxide; water; triethylamine; In acetone; 1: Addition / 2: Cyclization / 3: Decarboxylation;
DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M