Spiro[3H-indole-3,6'(4'aH)-[1H]pyrano[3,4-f]- indolizine]-4'-carboxylic acid,1,2,5',5'a,7',8',10',10'a-octahydro-1'- methyl-2-oxo-,methyl ester,(1'R,3R,4'aS,5'aR,10'aS)-

Base Information

• Chemical Name: Spiro[3H-indole-3,6'(4'aH)-[1H]pyrano[3,4-f]- indolizine]-4'-carboxylic acid,1,2,5',5'a,7',8',10',10'a-octahydro-1'- methyl-2-oxo-,methyl ester,(1'R,3R,4'aS,5'aR,10'aS)-
• CAS No.: 17507-92-5
• Molecular Formula: C₂₁H₂₄N₂O₄
• Molecular Weight: 368.433

Synonyms:

Chemical Property of Spiro[3H-indole-3,6'(4'aH)-[1H]pyrano[3,4-f]- indolizine]-4'-carboxylic acid,1,2,5',5'a,7',8',10',10'a-octahydro-1'- methyl-2-oxo-,methyl ester,(1'R,3R,4'aS,5'aR,10'aS)-

Chemical Property:

Purity/Quality:

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Useful:

Technology Process of Spiro[3H-indole-3,6'(4'aH)-[1H]pyrano[3,4-f]- indolizine]-4'-carboxylic acid,1,2,5',5'a,7',8',10',10'a-octahydro-1'- methyl-2-oxo-,methyl ester,(1'R,3R,4'aS,5'aR,10'aS)-

There total 7 articles about Spiro[3H-indole-3,6'(4'aH)-[1H]pyrano[3,4-f]- indolizine]-4'-carboxylic acid,1,2,5',5'a,7',8',10',10'a-octahydro-1'- methyl-2-oxo-,methyl ester,(1'R,3R,4'aS,5'aR,10'aS)- 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:

→ Mitraphyllin (509-80-8,4697-68-1,4963-01-3,5171-37-9,5629-60-7,6883-35-8,6899-73-6,14019-66-0,17507-91-4,17507-92-5,17507-93-6,17507-94-7,19775-85-0,19775-86-1,24196-09-6,24196-10-9,36001-48-6,52689-99-3,52690-00-3,131725-45-6,131725-46-7,134001-70-0)

Guidance literature:

/BRN= 631614/ = C22H26N2O4 (Hydrolyse).;

DOI:10.1021/ja00866a062

Reference yield:

→ Isomitraphyllin (509-80-8,4697-68-1,4963-01-3,5171-37-9,5629-60-7,6883-35-8,6899-73-6,14019-66-0,17507-91-4,17507-92-5,17507-93-6,17507-94-7,19775-85-0,19775-86-1,24196-09-6,24196-10-9,36001-48-6,52689-99-3,52690-00-3,131725-45-6,131725-46-7,134001-70-0)

Guidance literature:

Mitraphyllin + Py. (Erhitzen, 20 h).;

DOI:10.1021/jo01344a023

Reference yield:

→ Pteropodin (509-80-8,4697-68-1,4963-01-3,5171-37-9,5629-60-7,6883-35-8,6899-73-6,14019-66-0,17507-91-4,17507-92-5,17507-93-6,17507-94-7,19775-85-0,19775-86-1,24196-09-6,24196-10-9,36001-48-6,52689-99-3,52690-00-3,131725-45-6,131725-46-7,134001-70-0)

Guidance literature:

Indolin von Acetoxytetrahydroalstonin,HAc;

DOI:10.1016/S0031-9422(00)85816-1

Downstream raw materials:

mitraphylline

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