3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester
CAS No.:936132-64-8
Molecular Formula:C₂₄H₂₅N₃O₆
Molecular Weight:451.479
Hs Code.:

3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid <i>tert</i>-butyl ester

Synonyms:3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Suppliers and Price of 3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

There total 5 articles about 3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-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: 81.0%

: 882188-88-7
tert-butyl 3-formyl-1H-indazole-1-carboxylate

: 100945-15-1,88568-95-0
N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester

: 936132-64-8
3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at -84 - 20 ℃; for 3h;
DOI:10.1016/j.tetlet.2007.02.042

Reference yield:

: 351457-12-0
1H-indazole-3-carboxylic acid methoxy(methyl)amide

: 936132-64-8
3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / LiAlH₄ / tetrahydrofuran / 13 h / -15 - 20 °C

2: 100 percent / triethylamine; dimethylaminopyridine / CH₂Cl₂ / 13 h / 0 - 20 °C

3: 81 percent / 1,8-diazabicyclo[5,4,0]undec-7-ene / CH₂Cl₂ / 3 h / -84 - 20 °C

With dmap; lithium aluminium tetrahydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; dichloromethane; 3: Wittig-Horner reaction;
DOI:10.1016/j.tetlet.2007.02.042

Reference yield:

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

: 936132-64-8
3-(2-benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-indazole-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / triethylamine; dimethylaminopyridine / CH₂Cl₂ / 13 h / 0 - 20 °C

2: 81 percent / 1,8-diazabicyclo[5,4,0]undec-7-ene / CH₂Cl₂ / 3 h / -84 - 20 °C

With dmap; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In dichloromethane; 2: Wittig-Horner reaction;
DOI:10.1016/j.tetlet.2007.02.042