C₂₆H₂₆ClN₅O₇

Base Information

Chemical Name:C₂₆H₂₆ClN₅O₇
CAS No.:1622343-17-2
Molecular Formula:C₂₆H₂₆ClN₅O₇
Molecular Weight:555.975
Hs Code.:

C<sub>26</sub>H<sub>26</sub>ClN<sub>5</sub>O<sub>7</sub>

Synonyms:C₂₆H₂₆ClN₅O₇

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Chemical Property of C₂₆H₂₆ClN₅O₇

Chemical Property:

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Technology Process of C₂₆H₂₆ClN₅O₇

There total 13 articles about C₂₆H₂₆ClN₅O₇ 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:

: 1622396-81-9
C₂₁H₂₂ClN₃O₅

: 5-methyl-3-isoxazoleisocyanate

: 1622343-17-2
C₂₆H₂₆ClN₅O₇

Guidance literature:: In dichloromethane; at 20 ℃; for 5h;

Reference yield:

: 3943-74-6
4-hydroxy-3-methoxybenzoic acid methyl ester

: 1622343-17-2
C₂₆H₂₆ClN₅O₇

Guidance literature:: Multi-step reaction with 11 steps

1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 100 °C

2: nitric acid; acetic acid / 0.33 h / -10 °C

3: iron; ammonium chloride / water; methanol / 105 °C

4: ammonium acetate; methanol / 100 °C

5: methanesulfonic acid; trifluoroacetic acid / 3 h / Reflux

6: pyridine / 3 h / 120 °C

7: thionyl chloride / N,N-dimethyl-formamide / 1.5 h / Reflux

8: methanol; ammonia / dichloromethane / 0.17 h / 80 °C

9: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 3 h / 0 - 20 °C

10: caesium carbonate / tetrahydrofuran / 50 °C

11: dichloromethane / 5 h / 20 °C

With pyridine; methanol; thionyl chloride; methanesulfonic acid; di-isopropyl azodicarboxylate; ammonium acetate; ammonia; nitric acid; iron; potassium carbonate; ammonium chloride; caesium carbonate; acetic acid; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 56441-97-5
methyl 4-(benzyloxy)-3-methoxybenzoate

: 1622343-17-2
C₂₆H₂₆ClN₅O₇

Guidance literature:: Multi-step reaction with 10 steps

1: nitric acid; acetic acid / 0.33 h / -10 °C

2: iron; ammonium chloride / water; methanol / 105 °C

3: ammonium acetate; methanol / 100 °C

4: methanesulfonic acid; trifluoroacetic acid / 3 h / Reflux

5: pyridine / 3 h / 120 °C

6: thionyl chloride / N,N-dimethyl-formamide / 1.5 h / Reflux

7: methanol; ammonia / dichloromethane / 0.17 h / 80 °C

8: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 3 h / 0 - 20 °C

9: caesium carbonate / tetrahydrofuran / 50 °C

10: dichloromethane / 5 h / 20 °C

With pyridine; methanol; thionyl chloride; methanesulfonic acid; di-isopropyl azodicarboxylate; ammonium acetate; ammonia; nitric acid; iron; ammonium chloride; caesium carbonate; acetic acid; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;