6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-

Base Information Edit

Chemical Name:6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-
CAS No.:211750-50-4
Molecular Formula:C16H18N4O2
Molecular Weight:298.345
Hs Code.:
Mol file:211750-50-4.mol

Synonyms:6H-Dipyrido[3,2-b:2,3-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-

Suppliers and Price of 6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-

Supply Marketing:Edit

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

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Chemical Property of 6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl- Edit

Chemical Property:

PSA：72.94000
LogP:1.40010

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

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Technology Process of 6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-

There total 16 articles about 6H-Dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one,11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl- 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: 82.0%

: C₁₇H₁₈N₄O₃

: 211750-50-4
BIRK 122

Guidance literature:: With methanol; sodium tetrahydroborate; sodium ethanolate; at 40 ℃;

Reference yield: 80.0%

: 639469-43-5
INRF 105

: 211750-50-4
BIRK 122

Guidance literature:: With hydrogenchloride; sodium tetrahydroborate; In tetrahydrofuran; diethylene glycol dimethyl ether; at 0 - 25 ℃; for 6.5h; Reagent/catalyst; Inert atmosphere; Large scale;
DOI:10.1021/op8000756