N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

Base Information

Chemical Name:N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide
CAS No.:174362-30-2
Molecular Formula:C₂₈H₂₉NOS
Molecular Weight:427.61
Hs Code.:

Synonyms:N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

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Chemical Property of N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

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Technology Process of N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

There total 7 articles about N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide 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: 63.0%

: 142-29-0
cyclopentene

: 205494-66-2
N-((R)-1-Naphthalen-1-yl-ethyl)-N-((E)-3-phenyl-thioacryloyl)-acetamide

: 174362-30-2
N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

Guidance literature:: In acetone; for 1h; Ambient temperature;
DOI:10.1002/prac.19963380126

Reference yield:

: 3886-70-2
(R)-1-(1-Naphthyl)ethylamine

: 174362-30-2
N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / diethyl ether / 0 °C

2: 56 percent / P₄S₁₀ / tetrahydrofuran / 8 h / Ambient temperature

3: pyridine; CH₂Cl₂ / 4 h / Ambient temperature

With tetraphosphorus decasulfide; In tetrahydrofuran; pyridine; diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(98)00067-2

Reference yield:

: 205494-62-8
N-(R)-1-(1-naphthyl)ethyl cinnamamide

: 174362-30-2
N-((R)-1-Naphthalen-1-yl-ethyl)-N-((4R,4aR,7aR)-4-phenyl-4,4a,5,6,7,7a-hexahydro-cyclopenta[b]thiopyran-2-yl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / P₄S₁₀ / tetrahydrofuran / 8 h / Ambient temperature

2: pyridine; CH₂Cl₂ / 4 h / Ambient temperature

With tetraphosphorus decasulfide; In tetrahydrofuran; pyridine; dichloromethane;
DOI:10.1016/S0040-4020(98)00067-2