C₄₁H₅₅N₇O₇Si

Base Information

Chemical Name:C₄₁H₅₅N₇O₇Si
CAS No.:1620239-71-5
Molecular Formula:C₄₁H₅₅N₇O₇Si
Molecular Weight:786.016
Hs Code.:

C<sub>41</sub>H<sub>55</sub>N<sub>7</sub>O<sub>7</sub>Si

Synonyms:C₄₁H₅₅N₇O₇Si

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Chemical Property of C₄₁H₅₅N₇O₇Si

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Technology Process of C₄₁H₅₅N₇O₇Si

There total 16 articles about C₄₁H₅₅N₇O₇Si 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: 73.0%

: 1210418-70-4
tert-butyl ((3R,4R,5S)-1-(3-aminopyridin-4-yl)-4-{[tert-butyl(dimethyl)silyl]oxy}-5-methylpiperidin-3-yl)carbamate

: 1620239-66-8
3-{[(benzyloxy)carbonyl]amino}-7-ethoxy-1,8-naphthyridine-2-carboxylic acid

: 1620239-71-5
C₄₁H₅₅N₇O₇Si

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,2-dichloro-ethane; N,N-dimethyl-formamide; at 55 ℃; for 2h;

Reference yield:

: 13091-23-1
4-chloro-3-nitropyridine

: 1620239-71-5
C₄₁H₅₅N₇O₇Si

Guidance literature:: Multi-step reaction with 3 steps

1: isopropyl alcohol / 3 h / 90 °C

2: iron; acetic acid / 2 h / 20 °C

3: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide; 1,2-dichloro-ethane / 2 h / 55 °C

With iron; acetic acid; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,2-dichloro-ethane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1196156-67-8
2-amino-6-bromonicotinaldehydev

: 1620239-71-5
C₄₁H₅₅N₇O₇Si

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine / 32 h / 70 - 100 °C / Sealed tube

1.2: 16 h / 100 °C / Sealed tube

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 65 °C / Sealed tube

3.1: lithium hydroxide monohydrate / water; tetrahydrofuran / 2 h / 65 °C / Sealed tube

4.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide; 1,2-dichloro-ethane / 2 h / 55 °C

With pyridine; lithium hydroxide monohydrate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;