(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

Base Information

Chemical Name:(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol
CAS No.:663926-37-2
Molecular Formula:C₂₈H₃₈N₂O₄S
Molecular Weight:498.687
Hs Code.:

Synonyms:(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

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Chemical Property of (R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

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Technology Process of (R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

There total 7 articles about (R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol 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:

: 663926-42-9
4-tert-butoxy-2-isopropoxy-7-(R)-oxiranyl-benzothiazole

: 181657-56-7,404028-21-3,796038-32-9,181657-57-8
(1S,2S)-2-(benzyloxy)cyclopentanamine

: 663926-37-2
(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

Guidance literature:: In diethylene glycol dimethyl ether; at 115 ℃; for 17h;

Reference yield:

: 142596-59-6
1-tert-butoxy-4-fluoro-2-nitrobenzene

: 663926-37-2
(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogen / platinum(IV) oxide / methanol / 18 h

2.1: triethylamine / toluene / 18 h / 20 °C

2.2: 0.25 h / 0 °C

3.1: triethylamine / 48 h / Heating / reflux

4.1: tert.-butyl lithium; copper(I) cyanide; lithium chloride / tetrahydrofuran; pentane / 0.25 h / -78 - -20 °C

4.2: 1 h / 0 °C

5.1: borane-THF; (1R,2S)-1-Amino-2-indanol / tetrahydrofuran / 1.5 h / 20 °C

6.1: potassium carbonate / acetone / 48 h / Heating / reflux

7.1: diethylene glycol dimethyl ether / 17 h / 115 °C

With borane-THF; (1R,2S)-1-Amino-2-indanol; hydrogen; tert.-butyl lithium; copper(I) cyanide; potassium carbonate; triethylamine; lithium chloride; platinum(IV) oxide; In tetrahydrofuran; methanol; diethylene glycol dimethyl ether; acetone; toluene; pentane;

Reference yield:

: 862594-16-9
2-tert-butoxy-5-fluoroaniline

: 663926-37-2
(R)-2-((1S,2S)-2-benzyloxy-cyclopentylamino)-1-(4-tert-butoxy-2-isopropoxy-benzothiazol-7-yl)-ethanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / toluene / 18 h / 20 °C

1.2: 0.25 h / 0 °C

2.1: triethylamine / 48 h / Heating / reflux

3.1: tert.-butyl lithium; copper(I) cyanide; lithium chloride / tetrahydrofuran; pentane / 0.25 h / -78 - -20 °C

3.2: 1 h / 0 °C

4.1: borane-THF; (1R,2S)-1-Amino-2-indanol / tetrahydrofuran / 1.5 h / 20 °C

5.1: potassium carbonate / acetone / 48 h / Heating / reflux

6.1: diethylene glycol dimethyl ether / 17 h / 115 °C

With borane-THF; (1R,2S)-1-Amino-2-indanol; tert.-butyl lithium; copper(I) cyanide; potassium carbonate; triethylamine; lithium chloride; In tetrahydrofuran; diethylene glycol dimethyl ether; acetone; toluene; pentane;