N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

Base Information

Chemical Name:N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide
CAS No.:1392002-34-4
Molecular Formula:C₂₀H₂₁FN₄O₂
Molecular Weight:368.411
Hs Code.:

Synonyms:N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

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Chemical Property of N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

Chemical Property:

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Technology Process of N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

There total 3 articles about N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide 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: 49.0%

: 164648-60-6
1H-1,3-benzodiazol-6-ylmethanamine

: 530-62-1
1,1'-carbonyldiimidazole

: 3202-34-4
4-(4-Fluorophenoxy)piperidine hydrochloride

: 1392002-34-4
N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

Guidance literature:: 1H-1,3-benzodiazol-6-ylmethanamine; 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; for 1h;

4-(4-Fluorophenoxy)piperidine hydrochloride; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 16h;

Reference yield:

: 15788-16-6
5-benzimidazolecarboxylic acid

: 1392002-34-4
N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 96 h / 0 - 20 °C

2.1: diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 4 h / 20 °C

2.2: 96 h / 20 °C

3.1: N,N-dimethyl-formamide / 1 h

3.2: 16 h

With lithium aluminium tetrahydride; diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 106429-29-2
(1H-benzo[d]imidazol-6-yl)methanol

: 1392002-34-4
N-(1H-1,3-benzodiazol-6-ylmethyl)-4-(4-fluorophenoxy)piperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 4 h / 20 °C

1.2: 96 h / 20 °C

2.1: N,N-dimethyl-formamide / 1 h

2.2: 16 h

With diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide;