4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Base Information

Chemical Name:4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid
CAS No.:396725-70-5
Molecular Formula:C₃₁H₂₉NO₄S
Molecular Weight:511.642
Hs Code.:

4'-(4-<i>tert</i>-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Synonyms:4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

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Chemical Property of 4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Chemical Property:

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Technology Process of 4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

There total 6 articles about 4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid 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:

: 4'-{[1-(4-tert-Butoxycarbonylsulfanyl-phenyl)-meth-(E)-ylidene]-amino}-[1,1';2',1'']terphenyl-3-carboxylic acid

: 396725-70-5
4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Guidance literature:: With sodium tetrahydroborate; In dichloromethane; at 20 ℃;
DOI:10.1021/jm0103099

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 396725-70-5
4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 82 percent / DMAP; Et₃N / tetrahydrofuran / 20 °C

2: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

3: 516 mg / NaBH₄ / tetrahydrofuran / 1 h / 0 °C

4: 90 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -70 - 20 °C

5: AcOH / CH₂Cl₂ / 20 °C

6: NaBH₄ / CH₂Cl₂ / 20 °C

With dmap; sodium tetrahydroborate; oxalyl dichloride; acetic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; 4: Swern oxidation;
DOI:10.1021/jm0103099

Reference yield:

: 1074-36-8
4-mercaptobenzoic acid

: 396725-70-5
4'-(4-tert-butoxycarbonylsulfanyl-benzylamino)-[1,1';2',1'']terphenyl-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 82 percent / DMAP; Et₃N / tetrahydrofuran / 20 °C

2: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

3: 516 mg / NaBH₄ / tetrahydrofuran / 1 h / 0 °C

4: 90 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -70 - 20 °C

5: AcOH / CH₂Cl₂ / 20 °C

6: NaBH₄ / CH₂Cl₂ / 20 °C

With dmap; sodium tetrahydroborate; oxalyl dichloride; acetic acid; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; 4: Swern oxidation;
DOI:10.1021/jm0103099