(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

Base Information

Chemical Name:(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]
CAS No.:256451-62-4
Molecular Formula:C₁₈H₂₆N₂O₃S
Molecular Weight:350.482
Hs Code.:

Synonyms:(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

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Chemical Property of (3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

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Technology Process of (3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

There total 5 articles about (3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole] 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: 38.0%

: 4229-44-1
N-methylhydroxyamine hydrochloride

: 256451-57-7
(2S)-2-[N-(2-cyclopropylideneethyl)-N-tosylamino]-3-methylbutanal

: 256451-62-4
(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

: (3'aS,6'S,6'aS)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

Guidance literature:: With triethylamine; In tetrachloromethane; at 20 ℃;

Reference yield:

: 51220-85-0,21957-66-4
Methyl (S)-N-<(4-methylphenyl)sulfonyl>valinate

: 256451-62-4
(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / dppe; NaH / Pd(dba)2 / tetrahydrofuran / 12 h / 20 °C

2: 93 percent / DIBALH / CH₂Cl₂; hexane / 3 h / -78 °C

3: 98 percent / DMSO; oxalyl chloride; iPr₂EtN / CH₂Cl₂ / -78 - 20 °C

4: 24 percent / NEt₃ / CCl₄ / 20 °C

With oxalyl dichloride; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; 1,2-bis-(diphenylphosphino)ethane; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; tetrachloromethane; hexane; dichloromethane; 1: Substitution / 2: Reduction / 3: Oxidation / 4: Cycloaddition;

Reference yield:

: 32364-41-3
1-tosyloxy-1-vinylcyclopropane

: 256451-62-4
(3'aR,6'S,6'aR)-6'-isopropyl-1'-methyl-5'-tosylspiro[cyclopropane-1,3'-hexahydro-4H-pyrrolo[3,4-c]isoxazole]

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / dppe; NaH / Pd(dba)2 / tetrahydrofuran / 12 h / 20 °C

2: 93 percent / DIBALH / CH₂Cl₂; hexane / 3 h / -78 °C

3: 98 percent / DMSO; oxalyl chloride; iPr₂EtN / CH₂Cl₂ / -78 - 20 °C

4: 24 percent / NEt₃ / CCl₄ / 20 °C

With oxalyl dichloride; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; 1,2-bis-(diphenylphosphino)ethane; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; tetrachloromethane; hexane; dichloromethane; 1: Substitution / 2: Reduction / 3: Oxidation / 4: Cycloaddition;