C₃₇H₄₅N₇O₅

Base Information

Chemical Name:C₃₇H₄₅N₇O₅
CAS No.:1616889-70-3
Molecular Formula:C₃₇H₄₅N₇O₅
Molecular Weight:667.808
Hs Code.:

C<sub>37</sub>H<sub>45</sub>N<sub>7</sub>O<sub>5</sub>

Synonyms:C₃₇H₄₅N₇O₅

Suppliers and Price of C₃₇H₄₅N₇O₅

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₃₇H₄₅N₇O₅

Chemical Property:

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Technology Process of C₃₇H₄₅N₇O₅

There total 9 articles about C₃₇H₄₅N₇O₅ 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: 73.0%

: 1007882-12-3
(S)-tert-butyl 2-(5-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

: 1616889-69-0
C₁₉H₂₃BrN₄O₃

: 1616889-70-3
C₃₇H₄₅N₇O₅

Guidance literature:: With potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tricyclohexylphosphine; In 1,4-dioxane; at 140 ℃; Microwave irradiation;
DOI:10.1002/cmdc.201400045

Reference yield:

: C₁₄H₁₉N₃O₇S

: 1616889-70-3
C₃₇H₄₅N₇O₅

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: potassium carbonate; thiophenol / acetonitrile; dimethyl sulfoxide / 60 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

4: potassium hydroxide; water / methanol / 40 °C

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

6: ammonium acetate / Reflux; Molecular sieve

7: potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tricyclohexylphosphine / 1,4-dioxane / 140 °C / Microwave irradiation

With potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; ammonium acetate; water; potassium carbonate; thiophenol; N-ethyl-N,N-diisopropylamine; potassium hydroxide; tricyclohexylphosphine; In 1,4-dioxane; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; 7: |Suzuki Coupling;
DOI:10.1002/cmdc.201400045

Reference yield:

: 1616889-65-6
C₁₀H₁₈N₂O₃

: 1616889-70-3
C₃₇H₄₅N₇O₅

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

2: potassium hydroxide; water / methanol / 40 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

4: ammonium acetate / Reflux; Molecular sieve

5: potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tricyclohexylphosphine / 1,4-dioxane / 140 °C / Microwave irradiation

With potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; ammonium acetate; water; N-ethyl-N,N-diisopropylamine; potassium hydroxide; tricyclohexylphosphine; In 1,4-dioxane; methanol; dichloromethane; 5: |Suzuki Coupling;
DOI:10.1002/cmdc.201400045