(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

Base Information

Chemical Name:(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate
CAS No.:1425040-51-2
Molecular Formula:C₂₆H₃₄ClN₃O₇
Molecular Weight:536.025
Hs Code.:

Synonyms:(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

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Chemical Property of (3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

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Technology Process of (3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

There total 5 articles about (3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 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: 76.0%

: 1425040-20-5
tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate

: diethyl 3-propenylcyclopent-3-enedicarboxylate

: 1425040-51-2
(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

Guidance literature:: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate; diethyl 3-propenylcyclopent-3-enedicarboxylate; With C₆₄H₄₆NO₂P*Au⁽¹⁺⁾*C₂F₆NO₄S₂^(1-); In toluene; at -78 ℃; for 6h;

enantioselective reaction;
DOI:10.1021/ja3110472

Reference yield: 76.0%

: 1425040-20-5
tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate

: 119548-47-9
(2E)-2-butenyl-2-propynylpropanedionic acid diethyl ester

: 1425040-71-6
(3S,7aR)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

: 1425040-51-2
(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

Guidance literature:: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate; (2E)-2-butenyl-2-propynylpropanedionic acid diethyl ester; With C₆₄H₄₆NO₂P*Au⁽¹⁺⁾*C₂F₆NO₄S₂^(1-); In toluene; at 25 ℃; for 36h;

enantioselective reaction;
DOI:10.1021/ja3110472

Reference yield:

: 870-46-2
t-butoxycarbonylhydrazine

: 1425040-51-2
(3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: toluene / 4 h / 80 °C

2: N-Bromosuccinimide; pyridine / dichloromethane / 1 h / 25 °C

3: C₆₄H₄₆NO₂P*Au⁽¹⁺⁾*C₂F₆NO₄S₂^(1-) / toluene / 36 h / 25 °C

With pyridine; N-Bromosuccinimide; C₆₄H₄₆NO₂P*Au⁽¹⁺⁾*C₂F₆NO₄S₂^(1-); In dichloromethane; toluene; 3: |Diels-Alder Cycloaddition;
DOI:10.1021/ja3110472