4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

Base Information

Chemical Name:4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide
CAS No.:235101-11-8
Molecular Formula:C₁₇H₂₃N₃O₄S
Molecular Weight:365.453
Hs Code.:

Synonyms:4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

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Chemical Property of 4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

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Technology Process of 4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

There total 5 articles about 4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide 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: 57.0%

: 235101-03-8
1-carbethoxy-4-cyano-4-(benzyl)methanesulfonamidopiperidine

: 235101-11-8
4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

Guidance literature:: With sodium hydride; In acetonitrile; at 20 ℃;
DOI:10.1016/S0040-4020(99)00379-8

Reference yield:

: 100-39-0
benzyl bromide

: 235101-11-8
4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / NaH / dimethylformamide / 9 h / 20 °C

2: 57 percent / NaH / acetonitrile / 20 °C

With sodium hydride; In N,N-dimethyl-formamide; acetonitrile; 1: Addition / 2: Cyclization;
DOI:10.1016/S0040-4020(99)00379-8

Reference yield:

: 29976-53-2
N-ethoxycarbonyl-4-piperidone

: 235101-11-8
4-amino-1-benzyl-8-carbethoxy-1,8-diaza-2-thiaspiro[4.5]dec-3-ene 2,2-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / ammonium chloride; ammonium hydroxide / H₂O / 21 h

2: 85 percent / triethylamine / CH₂Cl₂ / 3.5 h / 0 °C

3: 54 percent / NaH / dimethylformamide / 9 h / 20 °C

4: 57 percent / NaH / acetonitrile / 20 °C

With ammonium hydroxide; ammonium chloride; sodium hydride; triethylamine; In dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; 1: Addition / 2: Acylation / 3: Addition / 4: Cyclization;
DOI:10.1016/S0040-4020(99)00379-8