(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

Base Information

Chemical Name:(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide
CAS No.:1226776-10-8
Molecular Formula:C₂₃H₂₉FN₂O₅
Molecular Weight:432.492
Hs Code.:

Synonyms:(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

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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)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

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Technology Process of (R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

There total 2 articles about (R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide 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: 91.0%

: 1226776-09-5
(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-hydroxypropionamide

: 74-88-4
methyl iodide

: 1226776-10-8
(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

Guidance literature:: With silver(l) oxide; In acetonitrile; at 20 ℃; for 96h; Inert atmosphere;
DOI:10.1021/jm100185c

Reference yield:

: 3262-72-4,3850-40-6,6368-20-3,90582-28-8,84311-18-2
(R)-N-tert-butoxycarbonyl serine

: 1262534-81-5
4-(((3'-fluoro)phenoxy)methyl)benzylamine hydrochloride

: 1226776-10-8
(R)-N-4'-(((3''-fluoro)phenoxy)methyl)benzyl 2-N-(tert-butoxycarbonyl)amino-3-methoxypropionamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / -78 °C / Inert atmosphere

1.2: 1.5 h / -78 - 20 °C / Inert atmosphere

2.1: silver(l) oxide / acetonitrile / 96 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; silver(l) oxide; isobutyl chloroformate; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jm200759t