5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester
CAS No.:256345-59-2
Molecular Formula:C₅₁H₆₁N₇O₈Si
Molecular Weight:928.173
Hs Code.:

5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

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Suppliers and Price of 5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

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Chemical Property of 5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

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Technology Process of 5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

There total 10 articles about 5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester 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: 56.0%

: 1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrazolyl-3-boronic acid

: 256345-55-8
5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-trifluoromethanesulfonyloxy-indazole-1-carboxylic acid tert-butyl ester

: 256345-59-2
5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; sodium carbonate; In ethanol; toluene; for 1.5h; Heating;
DOI:10.1016/S0960-894X(99)00564-8

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 256345-59-2
5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 79 percent / DMAP; Et₃N / CH₂Cl₂ / 1 h / 25 °C

2: 77 percent / NH₃ / methanol / 14 h / 25 °C

3: 79 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

4: 56 percent / (Ph₃P)4Pd; TBAB; Na₂CO₃ / toluene; ethanol / 1.5 h / Heating

With pyridine; dmap; tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; ammonia; sodium carbonate; triethylamine; In methanol; ethanol; dichloromethane; toluene; 1: t-Butoxycarbonylation / 2: Ammonolysis / 3: Triflation / 4: Arylation;
DOI:10.1016/S0960-894X(99)00564-8

Reference yield:

: 321-12-0
2-fluoro-5-methyl-benzoic acid

: 256345-59-2
5-[(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-7-(3-nitro-benzyl)-6-oxo-hexahydro-1,3-dioxa-5,7-diaza-azulen-5-ylmethyl]-3-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: aq. HCl / 14 h / Heating

2: 15 percent / NBS; (PhCO)2O₂ / CCl₄

3: 52 percent / acetonitrile / 48 h / Heating

4: 42 percent / NH₂NH₂ / butan-1-ol / 6 h / Heating

5: 79 percent / DMAP; Et₃N / CH₂Cl₂ / 1 h / 25 °C

6: 77 percent / NH₃ / methanol / 14 h / 25 °C

7: 79 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

8: 56 percent / (Ph₃P)4Pd; TBAB; Na₂CO₃ / toluene; ethanol / 1.5 h / Heating

With pyridine; hydrogenchloride; dmap; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; ammonia; sodium carbonate; triethylamine; hydrazine; dibenzoyl peroxide; In methanol; tetrachloromethane; ethanol; dichloromethane; toluene; acetonitrile; butan-1-ol; 1: Esterification / 2: Bromination / 3: Alkylation / 4: Condensation / 5: t-Butoxycarbonylation / 6: Ammonolysis / 7: Triflation / 8: Arylation;
DOI:10.1016/S0960-894X(99)00564-8