N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

Base Information

Chemical Name:N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide
CAS No.:1053266-43-5
Molecular Formula:C₃₁H₄₈N₆O₆Si₂
Molecular Weight:656.93
Hs Code.:

N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

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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 N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

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Technology Process of N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

There total 3 articles about N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide 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:

: 5432-17-7
3-ethoxybenzoic acid ethyl ester

: 1053266-43-5
N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / aq. 0.1 N NaOH / 1 h / Heating

2: DCC, N-hydroxysuccinimide / dimethylformamide / 30 h / Ambient temperature

With sodium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jm00019a014

Reference yield:

: 99-06-9
3-Carboxyphenol

: 1053266-43-5
N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / K₂CO₃ / dimethylformamide / 3 h / 60 °C

2: 90 percent / aq. 0.1 N NaOH / 1 h / Heating

3: DCC, N-hydroxysuccinimide / dimethylformamide / 30 h / Ambient temperature

With sodium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; potassium carbonate; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jm00019a014

Reference yield:

: 621-51-2
3-ethoxybenzoic acid

: 160056-49-5
2'-amino-2'-deoxy-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-adenosine

: 1053266-43-5
N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide

Guidance literature:: With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; for 30h; Ambient temperature;
DOI:10.1021/jm00019a014