C₃₆H₄₁N₃O₇

Base Information

Chemical Name:C₃₆H₄₁N₃O₇
CAS No.:1275620-48-8
Molecular Formula:C₃₆H₄₁N₃O₇
Molecular Weight:627.737
Hs Code.:

C<sub>36</sub>H<sub>41</sub>N<sub>3</sub>O<sub>7</sub>

Synonyms:C₃₆H₄₁N₃O₇

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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 C₃₆H₄₁N₃O₇

Chemical Property:

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Technology Process of C₃₆H₄₁N₃O₇

There total 15 articles about C₃₆H₄₁N₃O₇ 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:

: 1275620-47-7
C₃₇H₄₃N₃O₇

: 1275620-48-8
C₃₆H₄₁N₃O₇

Guidance literature:: C₃₇H₄₃N₃O₇; With lithium hydroxide; In tetrahydrofuran; at 20 ℃;

With hydrogenchloride; In tetrahydrofuran; water; pH=< 7;

Reference yield:

: 315701-04-3
2,3-dibromo-3-phenyl-1-(3-acetamido-2-benzofuryl)propan-1-one

: 1275620-48-8
C₃₆H₄₁N₃O₇

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium acetate / acetone

2.1: acetic acid; phosphoric acid / 5 h / Reflux

3.1: trichlorophosphate / 2 h / Reflux

4.1: sodium t-butanolate / dimethyl sulfoxide / 1 h / 0 - 20 °C

4.2: 4 h / 10 °C

4.3: pH 6 - 7

5.1: thionyl chloride / 1 h / Reflux

6.1: benzotriazol-1-ol; 4-methyl-morpholine; HATU / dichloromethane / 20 °C

7.1: lithium hydroxide / tetrahydrofuran / 20 °C

7.2: pH < 7

With 4-methyl-morpholine; thionyl chloride; phosphoric acid; potassium acetate; benzotriazol-1-ol; acetic acid; HATU; lithium hydroxide; sodium t-butanolate; trichlorophosphate; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; acetone;

Reference yield:

: 611-20-1
salicylonitrile

: 1275620-48-8
C₃₆H₄₁N₃O₇

Guidance literature:: Multi-step reaction with 11 steps

1.1: potassium carbonate / butanone / 0.5 h / 20 °C

1.2: 100 °C

2.1: ethanol; water / 5 - 10 °C

3.1: Warmed water bath

4.1: bromine / chloroform

5.1: potassium acetate / acetone

6.1: acetic acid; phosphoric acid / 5 h / Reflux

7.1: trichlorophosphate / 2 h / Reflux

8.1: sodium t-butanolate / dimethyl sulfoxide / 1 h / 0 - 20 °C

8.2: 4 h / 10 °C

8.3: pH 6 - 7

9.1: thionyl chloride / 1 h / Reflux

10.1: benzotriazol-1-ol; 4-methyl-morpholine; HATU / dichloromethane / 20 °C

11.1: lithium hydroxide / tetrahydrofuran / 20 °C

11.2: pH < 7

With 4-methyl-morpholine; thionyl chloride; phosphoric acid; bromine; potassium acetate; potassium carbonate; benzotriazol-1-ol; acetic acid; HATU; lithium hydroxide; sodium t-butanolate; trichlorophosphate; In tetrahydrofuran; ethanol; dichloromethane; chloroform; water; dimethyl sulfoxide; acetone; butanone;