(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

Base Information

Chemical Name:(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide
CAS No.:186181-83-9
Molecular Formula:C₂₀H₂₅N₅O₃S₂
Molecular Weight:447.582
Hs Code.:

Synonyms:(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

Chemical Property:

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Technology Process of (4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

There total 4 articles about (4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide 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:

: 186181-82-8
C₂₅H₃₃N₅O₅S₂

: 186181-83-9
(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 23 ℃; for 2h;
DOI:10.1021/jm030050p

Reference yield:

: 95-16-9
1,3-Benzothiazole

: 186181-83-9
(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: butyllithium / hexane; tetrahydrofuran / 0.5 h / -70 °C

1.2: hexane; tetrahydrofuran / 2 h / -70 - 20 °C

2.1: NaBH₄; methanol / 3 h / -30 °C

3.1: trifluoroacetic acid / CH₂Cl₂ / 2 h / 23 °C

With methanol; sodium tetrahydroborate; n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jm030050p

Reference yield:

: 140894-62-8
N^α-Boc-N^ω-tosylarginine N,O-dimethylamide

: 186181-83-9
(4S)-N-[[[4-amino-5-(2-benzothiazolyl)-5-hydroxypentyl]amino]iminomethyl]-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: butyllithium / hexane; tetrahydrofuran / 0.5 h / -70 °C

1.2: hexane; tetrahydrofuran / 2 h / -70 - 20 °C

2.1: NaBH₄; methanol / 3 h / -30 °C

3.1: trifluoroacetic acid / CH₂Cl₂ / 2 h / 23 °C

With methanol; sodium tetrahydroborate; n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jm030050p