methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Base Information

Chemical Name:methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate
CAS No.:1609201-63-9
Molecular Formula:C₂₈H₃₁F₄N₃O₆S
Molecular Weight:613.63
Hs Code.:

methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Synonyms:methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

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Chemical Property of methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

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Technology Process of methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

There total 12 articles about methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate 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:

: 1412976-22-7
methyl (1aR,7bS)-5-amino-1,1 a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

: 1609201-64-0
2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonyl chloride

: 1609201-63-9
methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃; for 3.5h;

Reference yield:

: 1609201-65-1
1-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-3-fluorobenzene

: 1609201-63-9
methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: chlorosulfonic acid / dichloromethane / 0.5 h / 20 °C / Cooling with ice

2: pyridine / dichloromethane / 3.5 h / 0 - 20 °C

With pyridine; chlorosulfonic acid; In dichloromethane;

Reference yield:

: 1609201-66-2
((R)-1-ethylpyrrolidin-3-yl)-[2-(3-fluorophenyl)ethyl]amine

: 1609201-63-9
methyl (1aR,7bS)-5-(2-{2-[N-((R)-1-ethylpyrrolidin-3-yl)-N-trifluoroacetylamino]ethyl}-4-fluorobenzenesulfonylamino)-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 2.5 h / 20 °C / Cooling with ice

2: chlorosulfonic acid / dichloromethane / 0.5 h / 20 °C / Cooling with ice

3: pyridine / dichloromethane / 3.5 h / 0 - 20 °C

With pyridine; chlorosulfonic acid; triethylamine; In dichloromethane;