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C52H66N4O10Si

Base Information
  • Chemical Name:C52H66N4O10Si
  • CAS No.:1268463-71-3
  • Molecular Formula:C52H66N4O10Si
  • Molecular Weight:935.202
  • Hs Code.:
C<sub>52</sub>H<sub>66</sub>N<sub>4</sub>O<sub>10</sub>Si

Synonyms:C52H66N4O10Si

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Chemical Property of C52H66N4O10Si
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Technology Process of C52H66N4O10Si

There total 11 articles about C52H66N4O10Si 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:
Guidance literature:
(4aS,11aR,12aS,13S)-8-amino-3,7-bis(benzyloxy)-4a-(tert-butyldimethylsilyloxy)-13-(dimethylamino)-5-hydroxy-10-methoxy-11a,12,12a,13-tetrahydrotetraceno[2,3-d]isoxazole-4,6(4aH,11H)-dione; Boc-L-Pro-H; With sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane; at 20 ℃; for 1h;
With sodium hydrogencarbonate; In water; 1,2-dichloro-ethane; pH=7; Phosphate buffer;
Guidance literature:
Multi-step reaction with 11 steps
1.1: 2,2,6,6-tetramethyl-piperidine; n-butyllithium / tetrahydrofuran / 2.5 h / 0 °C
1.2: 2 h / 25 °C
2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 25 °C
3.1: dmap; triethylamine / dichloromethane / 12 h / 25 °C
4.1: boron tribromide / dichloromethane / 1.5 h / -78 - 25 °C
5.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C
5.2: 20 °C
6.1: acetic anhydride; copper(II) nitrate hydrate / 3 h / 0 - 20 °C
7.1: sodium dithionite / water; tetrahydrofuran / 20 °C
8.1: dmap / N,N-dimethyl-formamide / 5 h / 20 °C
9.1: N,N,N,N,-tetramethylethylenediamine; diisopropylamine; n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C
9.2: 2 h / -100 - -20 °C
10.1: hydrogenchloride / 1,4-dioxane / 20 °C
11.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 1 h / 20 °C
11.2: pH 7 / Phosphate buffer
With 2,2,6,6-tetramethyl-piperidine; hydrogenchloride; dmap; n-butyllithium; sodium dithionite; oxalyl dichloride; copper(II) nitrate hydrate; N,N,N,N,-tetramethylethylenediamine; acetic anhydride; boron tribromide; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; triethylamine; diisopropylamine; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; hexanes; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 10 steps
1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 25 °C
2.1: dmap; triethylamine / dichloromethane / 12 h / 25 °C
3.1: boron tribromide / dichloromethane / 1.5 h / -78 - 25 °C
4.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C
4.2: 20 °C
5.1: acetic anhydride; copper(II) nitrate hydrate / 3 h / 0 - 20 °C
6.1: sodium dithionite / water; tetrahydrofuran / 20 °C
7.1: dmap / N,N-dimethyl-formamide / 5 h / 20 °C
8.1: N,N,N,N,-tetramethylethylenediamine; diisopropylamine; n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C
8.2: 2 h / -100 - -20 °C
9.1: hydrogenchloride / 1,4-dioxane / 20 °C
10.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 1 h / 20 °C
10.2: pH 7 / Phosphate buffer
With hydrogenchloride; dmap; n-butyllithium; sodium dithionite; oxalyl dichloride; copper(II) nitrate hydrate; N,N,N,N,-tetramethylethylenediamine; acetic anhydride; boron tribromide; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; triethylamine; diisopropylamine; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; hexanes; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
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