4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone

Base Information

• Chemical Name: 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone
• CAS No.: 1287216-50-5
• Molecular Formula: C₃₀H₃₆ClN₃O₅S
• Molecular Weight: 586.152

Synonyms:4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone

Chemical Property of 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone

Chemical Property:

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Technology Process of 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone

There total 6 articles about 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(3-chloro-2-methylphenyl)thiosemicarbazone 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: 26.44%

(10S)-10-(4-formylphenyl)dihydroartemisinin (1287216-57-2) + C8H10ClN3S (54418-99-4) → 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N4-(3-chloro-2-methylphenyl)thiosemicarbazone (1287216-50-5)

Guidance literature:

With acetic acid; In ethanol; at 20 ℃; for 2h;

DOI:10.3390/molecules16064527

Reference yield:

dihydroartemisinin-O-trifluoroacetic ester (286851-11-4) → 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N4-(3-chloro-2-methylphenyl)thiosemicarbazone (1287216-50-5)

Guidance literature:

Multi-step reaction with 2 steps

1: dichloromethane / 12 h / -5 - 0 °C

2: acetic acid / ethanol / 2 h / 20 °C

With acetic acid; In ethanol; dichloromethane;

DOI:10.3390/molecules16064527

Reference yield:

dihydroartemisinin (71939-50-9) → 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N4-(3-chloro-2-methylphenyl)thiosemicarbazone (1287216-50-5)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 24 h / -5 - 0 °C

2: dichloromethane / 12 h / -5 - 0 °C

3: acetic acid / ethanol / 2 h / 20 °C

With acetic acid; triethylamine; In ethanol; dichloromethane;

DOI:10.3390/molecules16064527

upstream raw materials:

dihydroartemisinin-O-trifluoroacetic ester

(10S)-10-(4-formylphenyl)dihydroartemisinin

C₈H₁₀ClN₃S

dihydroartemisinin

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