(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

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Chemical Name:(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate
CAS No.:1442445-52-4
Molecular Formula:C₃₀H₃₄Cl₂N₄O₃
Molecular Weight:569.531
Hs Code.:

Synonyms:(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

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Chemical Property of (R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

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Technology Process of (R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

There total 6 articles about (R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-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:

: 1442445-51-3
(R)-1-(1-(2,4-dichlorophenyl)ethyl)-6-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indazole

: 37784-17-1,59433-50-0
N-(tert-butoxycarbonyl)-D-proline

: 1442445-52-4
(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

Guidance literature:: With triethylamine; HATU; In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

: 1442445-49-9
(R)-6-bromo-1-(1-(2,4-dichlorophenyl)ethyl)-1H-indazole

: 1442445-52-4
(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; toluene / 18 h / 100 °C / Inert atmosphere

2: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

3: HATU; triethylamine / dichloromethane / 0.5 h / 20 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; triethylamine; HATU; trifluoroacetic acid; In dichloromethane; water; toluene;

Reference yield:

: 1442445-50-2
(R)-tert-butyl 4-(1-(1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-5,6-dihydropyridine-1(2H)-carboxylate

: 1442445-52-4
(R)-tert-butyl 2-(4-(1-((R)-1-(2,4-dichlorophenyl)ethyl)-1H-indazol-6-yl)-1,2,3 ,6-tetrahydropyridine-1-carbonyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

2: HATU; triethylamine / dichloromethane / 0.5 h / 20 °C

With triethylamine; HATU; trifluoroacetic acid; In dichloromethane;