methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

Base Information

Chemical Name:methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate
CAS No.:681247-66-5
Molecular Formula:C₂₈H₃₈FN₃O₅S
Molecular Weight:547.691
Hs Code.:

Synonyms:methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

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Chemical Property of methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

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Technology Process of methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

There total 8 articles about methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate 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: 74.0%

: 681247-65-4
methyl 2-({[2-bromo-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

: 201230-82-2
carbon monoxide

: 140-80-7
5-diethylamino-2-pentylamine

: 681247-66-5
methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; triethylamine; In tetrahydrofuran; at 120 ℃; for 16h; under 23271.7 Torr;
DOI:10.1021/jm0601001

Reference yield:

: 947-65-9
methyl 2-hydroxy-1-naphthoate

: 681247-66-5
methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: 70 percent / H₂ / Pd/C / methanol; H₂O / 2.5 h / 60 °C / 77572.2 Torr

2: pyridine / CH₂Cl₂ / -20 - 20 °C

3: 54.06 g / Cs₂CO₃; Pd(OAc)2; 4,5-bis-diphenylphosphanyl-9,9-dimethyl-9H-xanthene / dioxane / 4 h / 100 °C

4: 100 percent / aq. HCl / tetrahydrofuran / 1 h / 20 °C

5: pyridine / 20 °C

6: 74 percent / PdCl₂(dppf)*CH₂Cl₂; triethylamine / tetrahydrofuran / 16 h / 120 °C / 23271.7 Torr

With pyridine; hydrogenchloride; palladium diacetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; hydrogen; caesium carbonate; triethylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; methanol; dichloromethane; water; 3: Buchwald reaction;
DOI:10.1021/jm0601001

Reference yield:

: 351003-45-7
2-bromo-4-fluorobenzene-1-sulfonyl chloride

: 681247-66-5
methyl 2-({[2-({[4-(diethylamino)-1-methylbutyl]amino}carbonyl)-4-fluorophenyl]sulfonyl}amino)-5,6,7,8-tetrahydro-1-naphthalenecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 20 °C

2: 74 percent / PdCl₂(dppf)*CH₂Cl₂; triethylamine / tetrahydrofuran / 16 h / 120 °C / 23271.7 Torr

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; triethylamine; In tetrahydrofuran; pyridine;
DOI:10.1021/jm0601001