N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide

Base Information

• Chemical Name: N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide
• CAS No.: 891144-30-2
• Molecular Formula: C₂₉H₃₃N₃O₅S
• Molecular Weight: 535.664

Synonyms:N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide

Chemical Property of N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide

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Technology Process of N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide

There total 5 articles about N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ⁶-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide 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:

3,4,5,6-tetrahydro-(4S,5S)-2-benzyl-7-[(2-bromo)benzyl]-4,5-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide (862884-26-2) + benzylamine (100-46-9) → N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ6-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide (891144-30-2)

Guidance literature:

With 1,8-diazabicyclo[5.4.0]undec-7-ene; trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II); In tetrahydrofuran; at 150 ℃; for 1h;

DOI:10.1016/j.tet.2005.11.094

Reference yield:

(4S,5S)-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide (835920-63-3) → N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ6-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide (891144-30-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 97 percent / Ag₂O / CH₂Cl₂ / 1 h / 100 °C / microwave irradiation

2: 95 percent / K₂CO₃ / dimethylformamide / 60 °C

3: DBU / Herrmann's palladacycle / tetrahydrofuran / 1 h / 150 °C

With potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; silver(l) oxide; trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II); In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.tet.2005.11.094

Reference yield:

(4S,5S)-3,4,5,6-tetrahydro-2-(2-bromobenzyl)-4,5-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide (891143-53-6) → N-Benzyl-2-((3aS,8aS)-7-benzyl-2,2-dimethyl-6,6-dioxo-hexahydro-1,3-dioxa-6λ6-thia-5,7-diaza-azulen-5-ylmethyl)-benzamide (891144-30-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 95 percent / K₂CO₃ / dimethylformamide / 60 °C

2: DBU / Herrmann's palladacycle / tetrahydrofuran / 1 h / 150 °C

With potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II); In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1016/j.tet.2005.11.094

upstream raw materials:

3,4,5,6-tetrahydro-(4S,5S)-2-benzyl-7-[(2-bromo)benzyl]-4,5-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide

benzylamine

(4S,5S)-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide

(4S,5S)-3,4,5,6-tetrahydro-2-(2-bromobenzyl)-4,5-O-isopropylidene-1,2,7-thiadiazepine 1,1-dioxide

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