C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

Base Information

Chemical Name:C₂HF₃O₂*C₂₃H₂₉ClN₆O₅
CAS No.:1093800-34-0
Molecular Formula:C₂HF₃O₂*C₂₃H₂₉ClN₆O₅
Molecular Weight:618.997
Hs Code.:

C<sub>2</sub>HF<sub>3</sub>O<sub>2</sub>*C<sub>23</sub>H<sub>29</sub>ClN<sub>6</sub>O<sub>5</sub>

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Chemical Property of C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

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Technology Process of C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

There total 4 articles about C₂HF₃O₂*C₂₃H₂₉ClN₆O₅ 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:

: 1093799-53-1
C₇H₆ClN₃O₂

: 1093800-34-0
C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 0.08 h / 20 °C

1.2: 15 h / 100 °C

1.3: 3 h / 20 - 30 °C

2.1: magnesium sulfate / N,N-dimethyl acetamide; acetonitrile / 80 °C

3.1: dichloromethane / 15 h / 20 °C

With magnesium sulfate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl acetamide; acetonitrile;

Reference yield:

: 1093799-83-7
C₇H₄Br₂ClN₃O₂

: 1093800-34-0
C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid; zinc / 0 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 0.08 h / 20 °C

2.2: 15 h / 100 °C

2.3: 3 h / 20 - 30 °C

3.1: magnesium sulfate / N,N-dimethyl acetamide; acetonitrile / 80 °C

4.1: dichloromethane / 15 h / 20 °C

With magnesium sulfate; acetic acid; N-ethyl-N,N-diisopropylamine; zinc; In dichloromethane; N,N-dimethyl acetamide; acetonitrile;

Reference yield:

: 90057-08-2
4-chloro-2-methoxy-1H-pyrrolo[2,3-d]pyrimidine

: 1093800-34-0
C₂HF₃O₂*C₂₃H₂₉ClN₆O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridinium hydrobromide perbromide / tert-butyl alcohol / 20 °C

2.1: acetic acid; zinc / 0 - 20 °C

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 0.08 h / 20 °C

3.2: 15 h / 100 °C

3.3: 3 h / 20 - 30 °C

4.1: magnesium sulfate / N,N-dimethyl acetamide; acetonitrile / 80 °C

5.1: dichloromethane / 15 h / 20 °C

With pyridinium hydrobromide perbromide; magnesium sulfate; acetic acid; N-ethyl-N,N-diisopropylamine; zinc; In dichloromethane; N,N-dimethyl acetamide; acetonitrile; tert-butyl alcohol;