4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

Base Information

Chemical Name:4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid
CAS No.:365282-11-7
Molecular Formula:C₃₁H₃₂N₄O₆S₂
Molecular Weight:620.75
Hs Code.:

Synonyms:4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

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Chemical Property of 4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

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Technology Process of 4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

There total 5 articles about 4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric 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: 86.0%

: 778567-09-2
4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid methyl ester

: 365282-11-7
4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; for 16h;
DOI:10.1021/jm010097f

Reference yield:

: 365281-96-5
(2-oxotetrahydro-thiophen-3-ylamino)-acetic acid tert-butyl ester

: 365282-11-7
4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: 67 percent / pyridine / 20 °C

2.1: MeONa / 0.5 h

2.2: methanol / 16 h

3.1: 68 percent / TFA / CH₂Cl₂ / 4 h

4.1: EDC; HOBt; NMM / CH₂Cl₂ / 0.33 h

4.2: 86 percent / CH₂Cl₂ / 15 h

5.1: 86 percent / aq. LiOH / tetrahydrofuran / 16 h

With 4-methyl-morpholine; pyridine; lithium hydroxide; sodium methylate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm010097f

Reference yield:

: 257933-90-7
[(4-methoxy-benzenesulfonyl)-(2-oxo-tetrahydrothiophen-3-yl)-amino]-acetic acid tert-butyl ester

: 365282-11-7
4-benzylsulfanyl-2-[{[(di-pyridin-2-yl-methyl)-carbamoyl]-methyl}-(4-methoxy-benzenesulfonyl)-amino]-butyric acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: MeONa / 0.5 h

1.2: methanol / 16 h

2.1: 68 percent / TFA / CH₂Cl₂ / 4 h

3.1: EDC; HOBt; NMM / CH₂Cl₂ / 0.33 h

3.2: 86 percent / CH₂Cl₂ / 15 h

4.1: 86 percent / aq. LiOH / tetrahydrofuran / 16 h

With 4-methyl-morpholine; lithium hydroxide; sodium methylate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm010097f