2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

Base Information

Chemical Name:2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide
CAS No.:865169-38-6
Molecular Formula:C₂₀H₂₂ClN₃O₃
Molecular Weight:387.866
Hs Code.:

2-amino-<i>N</i>-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

Synonyms:2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

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Chemical Property of 2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

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Technology Process of 2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

There total 3 articles about 2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide 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:

: 934264-70-7
tert-butyl (1-(benzo[d][1,3]dioxol-5-ylmethyl)piperidin-4-yl)carbamate

: 865169-38-6
2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: TFA / CH₂Cl₂ / 1 h / 0 °C

2: acetonitrile / 24 h / 80 °C

With trifluoroacetic acid; In dichloromethane; acetonitrile;
DOI:10.1021/jm0512286

Reference yield:

: 120-57-0,30024-74-9
piperonal

: 865169-38-6
2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 9.00 g / AcOH; sodium sulfate; sodium triacetoxyborohydride / tetrahydrofuran / 16 h

2: TFA / CH₂Cl₂ / 1 h / 0 °C

3: acetonitrile / 24 h / 80 °C

With sodium tris(acetoxy)borohydride; acetic acid; sodium sulfate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0512286

Reference yield:

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 865169-38-6
2-amino-N-(1-benzo[1,3]dioxol-5-ylmethyl-piperidin-4-yl)-5-chloro-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 9.00 g / AcOH; sodium sulfate; sodium triacetoxyborohydride / tetrahydrofuran / 16 h

2: TFA / CH₂Cl₂ / 1 h / 0 °C

3: acetonitrile / 24 h / 80 °C

With sodium tris(acetoxy)borohydride; acetic acid; sodium sulfate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0512286