1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

Base Information

Chemical Name:1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione
CAS No.:1416209-46-5
Molecular Formula:C₂₇H₂₄N₆O₂S
Molecular Weight:496.593
Hs Code.:

Synonyms:

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Chemical Property of 1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

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Technology Process of 1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

There total 5 articles about 1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione 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:

: 27038-81-9
8-(hydroxymethyl)-3-methyl-3,7-dihydro-1H-purine-2,6-dione

: 1416209-46-5
1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide / water / Heating

1.2: 2 h / Reflux

2.1: thionyl chloride / 6 h / Reflux

3.1: potassium hydroxide / water; N,N-dimethyl-formamide / 15 °C

4.1: potassium hydroxide / water; N,N-dimethyl-formamide / Reflux

4.2: 2 h

With thionyl chloride; potassium hydroxide; sodium hydroxide; In water; N,N-dimethyl-formamide; 4.1: |Thorpe Reaction;
DOI:10.1007/s10593-012-1149-1

Reference yield:

: 1416209-36-3
2-({[3-methyl-2,6-dioxo-7-(2-oxo-2-phenylethyl)-2,3,6,7-tetrahydro-1H-purin-8-yl]methyl}thio)-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine-3-carbonitrile

: 1416209-46-5
1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

Guidance literature:: 2-({[3-methyl-2,6-dioxo-7-(2-oxo-2-phenylethyl)-2,3,6,7-tetrahydro-1H-purin-8-yl]methyl}thio)-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine-3-carbonitrile; With potassium hydroxide; In water; N,N-dimethyl-formamide; Reflux;

With acetic acid; In water; N,N-dimethyl-formamide; for 2h;
DOI:10.1007/s10593-012-1149-1

Reference yield:

: 953079-61-3
C₁₅H₁₄N₄O₄

: 1416209-46-5
1-methyl-7-phenyl-10,11,12,13,14,15-hexahydro-1H-cycloocta[5'',6'']pyrido[3'',2'':4',5']thieno-[3',2':5,6][1,4]diazepino[7,1-f]purine-2,4(3H,6H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / 6 h / Reflux

2.1: potassium hydroxide / water; N,N-dimethyl-formamide / 15 °C

3.1: potassium hydroxide / water; N,N-dimethyl-formamide / Reflux

3.2: 2 h

With thionyl chloride; potassium hydroxide; In water; N,N-dimethyl-formamide; 3.1: |Thorpe Reaction;
DOI:10.1007/s10593-012-1149-1