trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

Base Information

Chemical Name:trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester
CAS No.:890657-32-6
Molecular Formula:C₂₀H₂₆F₃NO₈S
Molecular Weight:497.49
Hs Code.:

trifluoro-methanesulfonic acid 2-(6-<i>tert</i>-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

Synonyms:trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

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Chemical Property of trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

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Technology Process of trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

There total 4 articles about trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester 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:

: 2-tributylstannyl-N-Boc-3,4,5-trimethoxyaniline

: 890657-32-6
trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / CuI; P(2-furyl)3 / Pd₂(dba)3*CHCl₃ / 1-methyl-pyrrolidin-2-one / 2 h / 80 °C

2: 77 percent / L-Selectride / tetrahydrofuran / -78 - 20 °C

3: 404 mg / tetrahydrofuran / -78 - 20 °C

With copper(l) iodide; trifuran-2-yl-phosphane; L-Selectride; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one;
DOI:10.1021/ol0606536

Reference yield:

: 33948-35-5
2-iodo-cyclopent-2-enone

: 890657-32-6
trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / CuI; P(2-furyl)3 / Pd₂(dba)3*CHCl₃ / 1-methyl-pyrrolidin-2-one / 2 h / 80 °C

2: 77 percent / L-Selectride / tetrahydrofuran / -78 - 20 °C

3: 404 mg / tetrahydrofuran / -78 - 20 °C

With copper(l) iodide; trifuran-2-yl-phosphane; L-Selectride; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one;
DOI:10.1021/ol0606536

Reference yield:

: 890657-40-6
[3,4,5-trimethoxy-2-(5-oxo-cyclopent-1-enyl)-phenyl]-carbamic acid tert-butyl ester

: 890657-32-6
trifluoro-methanesulfonic acid 2-(6-tert-butoxycarbonylamino-2,3,4-trimethoxy-phenyl)-cyclopent-1-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / L-Selectride / tetrahydrofuran / -78 - 20 °C

2: 404 mg / tetrahydrofuran / -78 - 20 °C

With L-Selectride; In tetrahydrofuran;
DOI:10.1021/ol0606536