tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

Base Information

Chemical Name:tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate
CAS No.:1394898-81-7
Molecular Formula:C₂₁H₂₈ClN₅O₂
Molecular Weight:417.939
Hs Code.:

Synonyms:tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

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Chemical Property of tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

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Technology Process of tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

There total 1 articles about tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate 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:

: 84194-36-5
2-chloro-4-fluorobenzaldehyde

: 1394898-81-7
tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 20 °C

1.2: 3 h / 80 °C

2.1: triethylamine / dichloromethane / 1 h / 20 °C

2.2: 18 h / 20 °C

2.3: 1 h / 20 °C

With sodium hydride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1124/dmd.113.051839

Reference yield: 99.0%

: 1394898-81-7
tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

: 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; water; at 20 ℃; for 2h;
DOI:10.1124/dmd.113.051839

Reference yield:

: 1394898-81-7
tert-butyl 2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonane-7-carboxylate

: 1383719-97-8
1-(2-(2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl)-2,7-diazaspiro[3.5]nonan-7-yl)-2-(2-methylimidazo[2,1-b]thiazol-6-yl)ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane

2: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With hydrogenchloride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.05.024