benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

Base Information

Chemical Name:benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester
CAS No.:367506-70-5
Molecular Formula:C₁₈H₈N₄O₄
Molecular Weight:344.286
Hs Code.:

Synonyms:benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

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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 benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

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Technology Process of benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

There total 2 articles about benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester 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: 46.0%

: 17220-38-1
3,4-diaminofurazan

: 367506-67-0
benzoic acid 2,2-dihydroxy-1,3-dioxo-indan-4-yl ester

: 367506-70-5
benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

Guidance literature:: With acetic acid; In ethanol; at 20 ℃; for 18h;
DOI:10.1002/jhet.5570380514

Reference yield:

: 59725-61-0
4-(benzyloxy)-1-indanone

: 367506-70-5
benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / DMSO; NBS / 7 h / 60 - 80 °C

2: 46 percent / glacial AcOH / ethanol / 18 h / 20 °C

With N-Bromosuccinimide; acetic acid; dimethyl sulfoxide; In ethanol;
DOI:10.1002/jhet.5570380514

Reference yield:

: 367506-70-5
benzoic acid 9-oxo-9H-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-8-yl ester

: 8-benzyloxy-2-oxa-1,3,4,10-tetraazacyclopenta[b]fluoren-9-one

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / Cs₂CO₃ / tetrahydrofuran / 120 h / 20 °C

2: 27 percent / Et₃N; PPh₃; DEAD / tetrahydrofuran / 18 h / 20 °C

With caesium carbonate; triethylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 2: Mitsunobu reaction;
DOI:10.1002/jhet.5570380514