5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

Base Information

Chemical Name:5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid
CAS No.:1609122-58-8
Molecular Formula:C₂₄H₂₆F₂N₂O₅S
Molecular Weight:492.544
Hs Code.:

Synonyms:5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

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Chemical Property of 5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

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Technology Process of 5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

There total 19 articles about 5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic 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:

: 1609122-82-8
methyl 5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

: 1609122-58-8
5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; water; In 1,4-dioxane; at 100 ℃; for 22h; Inert atmosphere;

Reference yield:

: 1609122-73-7
methyl 5-amino-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate

: 1609122-58-8
5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 72 h / 20 °C

2: potassium carbonate; water / methanol / 1 h / 45 °C

3: sodium tris(acetoxy)borohydride / dichloromethane / 20 h / 20 °C

4: lithium hydroxide monohydrate; water / 1,4-dioxane / 22 h / 100 °C / Inert atmosphere

With pyridine; lithium hydroxide monohydrate; water; sodium tris(acetoxy)borohydride; potassium carbonate; In 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 1609122-78-2
methyl 2-(2,2-dimethylpropionylamino)-4-fluoro-6-hydroxybenzoate

: 1609122-58-8
5-[2-((R)-1-ethylpyrrolidin-3-ylmethyl)-4-fluorobenzene-sulfonylamino]-7-fluoro-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid

Guidance literature:: Multi-step reaction with 9 steps

1.1: potassium carbonate / toluene; acetone / 20 h / Reflux

2.1: bis[(trifluoromethanesulfonyl)imidate]-2-(dicyclohexyl(2’,6’-dimethoxybiphenyl))phosphine gold(I) / toluene / 3 h / 85 °C

3.1: sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride / water; dichloromethane / 2 h / 50 °C

4.1: sulfuric acid; methanol / 24 h / Reflux

4.2: 24 h / Reflux

5.1: zinc; ammonium chloride / 20 h / 85 °C / Inert atmosphere

6.1: pyridine / dichloromethane / 72 h / 20 °C

7.1: potassium carbonate; water / methanol / 1 h / 45 °C

8.1: sodium tris(acetoxy)borohydride / dichloromethane / 20 h / 20 °C

9.1: lithium hydroxide monohydrate; water / 1,4-dioxane / 22 h / 100 °C / Inert atmosphere

With pyridine; methanol; lithium hydroxide monohydrate; sulfuric acid; bis[(trifluoromethanesulfonyl)imidate]-2-(dicyclohexyl(2’,6’-dimethoxybiphenyl))phosphine gold(I); N-benzyl-N,N,N-triethylammonium chloride; water; sodium tris(acetoxy)borohydride; potassium carbonate; ammonium chloride; sodium hydroxide; zinc; In 1,4-dioxane; methanol; dichloromethane; water; acetone; toluene;