(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Base Information

Chemical Name:(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide
CAS No.:114614-40-3
Molecular Formula:C₂₀H₃₄ClN₃O₅
Molecular Weight:431.96
Hs Code.:

Synonyms:(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Suppliers and Price of (R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

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

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Chemical Property of (R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Chemical Property:

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Technology Process of (R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

There total 3 articles about (R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>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: 61.0%

: 38339-95-6
4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide

: 114614-79-8
(R)-2-<2-(methoxyethoxy)methoxy>propanol

: 114614-40-3
(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran;
DOI:10.1021/jm00403a011

Reference yield:

: 364-62-5
metoclopramide

: 114614-40-3
(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / sodium hydride, ethanethiol / dimethylformamide / 1.5 h / 100 - 105 °C

2: 61 percent / triphenylphosphine, diethyl azodicarboxylate / tetrahydrofuran

With sodium hydride; triphenylphosphine; ethanethiol; diethylazodicarboxylate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm00403a011

Reference yield:

: 114614-78-7
(R)-2-<2-(methoxyethoxy)methoxy>propionic acid methyl ester

: 114614-40-3
(R)-4-amino-5-chloro-N-<2-(diethylamino)ethyl>-2-<2-(methoxyethoxy)propoxy>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 91.5 percent / LAH / diethyl ether / 16 h

2: 61 percent / triphenylphosphine, diethyl azodicarboxylate / tetrahydrofuran

With lithium aluminium tetrahydride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jm00403a011