C₁₅H₁₈N₂O₅

Base Information

Chemical Name:C₁₅H₁₈N₂O₅
CAS No.:1372722-21-8
Molecular Formula:C₁₅H₁₈N₂O₅
Molecular Weight:306.318
Hs Code.:

C<sub>15</sub>H<sub>18</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C₁₅H₁₈N₂O₅

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Chemical Property of C₁₅H₁₈N₂O₅

Chemical Property:

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Technology Process of C₁₅H₁₈N₂O₅

There total 5 articles about C₁₅H₁₈N₂O₅ 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:

: 484664-62-2
(+/-)-trans-pyrrolidine-2,5-dicarboxamide

: 1372722-21-8
C₁₅H₁₈N₂O₅

Guidance literature:: Multi-step reaction with 3 steps

1: Rhodococcus erythropolis AJ₂₇₀ cells / 1 h / 30 °C / aq. phosphate buffer; Resolution of racemate; Enzymatic reaction

2: sodium hydrogencarbonate / ethanol; water / 20 °C

3: thionyl chloride / 4 h / 20 °C

With thionyl chloride; sodium hydrogencarbonate; In ethanol; water;
DOI:10.1021/jo300412j

Reference yield:

: C₆H₇N₃

: 1372722-21-8
C₁₅H₁₈N₂O₅

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid; water

2: Rhodococcus erythropolis AJ₂₇₀ cells / 1 h / 30 °C / aq. phosphate buffer; Resolution of racemate; Enzymatic reaction

3: sodium hydrogencarbonate / ethanol; water / 20 °C

4: thionyl chloride / 4 h / 20 °C

With thionyl chloride; sulfuric acid; water; sodium hydrogencarbonate; In ethanol; water;
DOI:10.1021/jo300412j

Reference yield:

: 1372722-17-2
(2R,5R)-5-carbamoylpyrrolidine-2-carboxylic acid

: 1372722-21-8
C₁₅H₁₈N₂O₅

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / ethanol; water / 20 °C

2: thionyl chloride / 4 h / 20 °C

With thionyl chloride; sodium hydrogencarbonate; In ethanol; water;
DOI:10.1021/jo300412j