4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin

Base Information

Chemical Name:4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin
CAS No.:152833-13-1
Molecular Formula:C₃₃H₃₆N₂O₇
Molecular Weight:572.658
Hs Code.:
Mol file:152833-13-1.mol

Synonyms:Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one,5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[1-(phenylmethyl)-4-piperidinyl]amino]-,[5R-(5a,5ab,8aa,9b)]-

Suppliers and Price of 4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of 4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin

Chemical Property:

Purity/Quality:

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Technology Process of 4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin

There total 2 articles about 4'-O-demethyl-4-((4''-(1''-benzylpiperidinyl))amino)-4-desoxypodophyllotoxin 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: 13.1%

: 16477-16-0
4'-O-demethyl-4β-bromo-4-desoxypodophyllotoxin

: 50541-93-0
4-amino-1-benzylpiperidine

: 152833-13-1
4'-O-demethyl-4β-{[4''-(1''-benzylpiperidinyl)]amino}-4-desoxypodophyllotoxin

Guidance literature:: In tetrahydrofuran; for 6h; Heating;
DOI:10.1021/jm00030a003

Reference yield:

: 6559-91-7
4'-demethylepipodophyllotoxin

: 152833-13-1
4'-O-demethyl-4β-{[4''-(1''-benzylpiperidinyl)]amino}-4-desoxypodophyllotoxin

Guidance literature:: Multi-step reaction with 2 steps

1: 11.5 g / HBr(gas) / CH₂Cl₂ / 2 h / 0 °C

2: 13.1 percent / tetrahydrofuran / 6 h / Heating

With hydrogen bromide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00030a003