C₄₁H₄₁N₃O₇S

Base Information

Chemical Name:C₄₁H₄₁N₃O₇S
CAS No.:1311298-79-9
Molecular Formula:C₄₁H₄₁N₃O₇S
Molecular Weight:719.858
Hs Code.:

C<sub>41</sub>H<sub>41</sub>N<sub>3</sub>O<sub>7</sub>S

Synonyms:C₄₁H₄₁N₃O₇S

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Chemical Property of C₄₁H₄₁N₃O₇S

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Technology Process of C₄₁H₄₁N₃O₇S

There total 9 articles about C₄₁H₄₁N₃O₇S 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:

: 108-30-5
succinic acid anhydride

: 1311298-77-7
N-[3-(4,4'-dimethoxytrityloxymethyl)benzyl]-N'-[(6-hydroxymethylpyridine-2-yl)methyl]thiourea

: 1311298-79-9
C₄₁H₄₁N₃O₇S

Guidance literature:: With dmap; In pyridine; at 20 ℃; for 72h;

Reference yield:

: 5453-67-8
2,6-bis(methoxycarbonyl)pyridine

: 1311298-79-9
C₄₁H₄₁N₃O₇S

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium borohydride / tetrahydrofuran / 16 h / Inert atmosphere

2.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

2.2: 12 h

3.1: carbon tetrabromide; triethylamine; sodium azide; triphenylphosphine / N,N-dimethyl-formamide / 25 h / Inert atmosphere

4.1: hydrogen / 5%-palladium/activated carbon / methanol / 5 h / 20 °C

5.1: chloroform-d1 / 5 h / Inert atmosphere; Reflux

6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

7.1: dmap / pyridine / 72 h / 20 °C

With dmap; lithium borohydride; sodium azide; carbon tetrabromide; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; triethylamine; triphenylphosphine; 5%-palladium/activated carbon; In tetrahydrofuran; pyridine; methanol; chloroform-d1; N,N-dimethyl-formamide;

Reference yield:

: 150058-64-3
(6-(((tert-butyldimethylsilyl)oxy)methyl)pyridin-2-yl)methanol

: 1311298-79-9
C₄₁H₄₁N₃O₇S

Guidance literature:: Multi-step reaction with 5 steps

1: carbon tetrabromide; triethylamine; sodium azide; triphenylphosphine / N,N-dimethyl-formamide / 25 h / Inert atmosphere

2: hydrogen / 5%-palladium/activated carbon / methanol / 5 h / 20 °C

3: chloroform-d1 / 5 h / Inert atmosphere; Reflux

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

5: dmap / pyridine / 72 h / 20 °C

With dmap; sodium azide; carbon tetrabromide; tetrabutyl ammonium fluoride; hydrogen; triethylamine; triphenylphosphine; 5%-palladium/activated carbon; In tetrahydrofuran; pyridine; methanol; chloroform-d1; N,N-dimethyl-formamide;