methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

Base Information

Chemical Name:methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate
CAS No.:199535-55-2
Molecular Formula:C₂₁H₃₁N₃O₇
Molecular Weight:437.493
Hs Code.:

Synonyms:methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

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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 methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

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Technology Process of methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

There total 3 articles about methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate 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: 64.0%

: 145013-05-4
tert-butyl N-({[(tert-butoxy)carbonyl]amino}methanethioyl)carbamate

: 775266-91-6
3-Amino-4-(2-hydroxy-ethyl)-benzoic acid methyl ester

: 199535-55-2
methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

Guidance literature:: With triethylamine; mercury dichloride; In N,N-dimethyl-formamide; 1.) 0 deg C, 0.5 h, 2.) RT, 24 h;
DOI:10.1021/jm970479e

Reference yield:

: 134403-90-0
4-(2-hydroxyethyl)-3-nitrobenzoic acid

: 199535-55-2
methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / H₂ / PtO₂ / ethanol / 3 h / 1551.4 Torr

2: 91 percent / acetyl chloride / Ambient temperature

3: 64 percent / Et₃N, HgCl₂ / dimethylformamide / 1.) 0 deg C, 0.5 h, 2.) RT, 24 h

With hydrogen; triethylamine; acetyl chloride; mercury dichloride; platinum(IV) oxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm970479e

Reference yield:

: 199535-47-2
3-amino-4-(2-hydroxyethyl)benzoic acid

: 199535-55-2
methyl 3-({[(tert-butoxycarbonyl)amino][(tert-butoxycarbonyl)imino]methyl}amino)-4-(2-hydroxyethyl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / acetyl chloride / Ambient temperature

2: 64 percent / Et₃N, HgCl₂ / dimethylformamide / 1.) 0 deg C, 0.5 h, 2.) RT, 24 h

With triethylamine; acetyl chloride; mercury dichloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm970479e