(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

Base Information

Chemical Name:(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone
CAS No.:117498-54-1
Molecular Formula:C₂₀H₂₄N₄O₆S
Molecular Weight:448.5
Hs Code.:

(4-amino-3-nitrophenyl)<4-<<N-<2-<(tert-butoxycarbonyl)amino>ethyl>carbamoyl>methyl>2-thienyl>methanone

Synonyms:(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

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Chemical Property of (4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

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Technology Process of (4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

There total 4 articles about (4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone 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: 41.0%

: 57260-73-8
N-BOC-1,2-diaminoethane

: 117498-95-0
[5-(4-Amino-3-nitro-benzoyl)-thiophen-3-yl]-acetic acid methyl ester

: 117498-54-1
(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

Guidance literature:: With 2-hydroxypyridin; at 120 ℃; for 2h;
DOI:10.1021/jm00122a020

Reference yield:

: 117498-53-0
<4-(carbomethoxymethyl)-2-thienyl>(4-chloro-3-nitrophenyl)methanone

: 117498-54-1
(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 43 percent / ammonia (g) / dimethylsulfoxide / 3.5 h / 85 °C

2: 41 percent / 2-hydroxypyridine / 2 h / 120 °C

With 2-hydroxypyridin; ammonia; In dimethyl sulfoxide;
DOI:10.1021/jm00122a020

Reference yield:

: 96-99-1
4-chloro-3-nitrobenzoate

: 117498-54-1
(4-amino-3-nitrophenyl)<4-<ethyl>carbamoyl>methyl>2-thienyl>methanone

Guidance literature:: Multi-step reaction with 5 steps

1: thionyl chloride, DMF / CHCl₃

2: 35.8 g / AlCl₃ / CH₂Cl₂ / 1.5 h / Heating

3: 75 percent / hydrogen chloride (g) / 1.5 h / Heating

4: 43 percent / ammonia (g) / dimethylsulfoxide / 3.5 h / 85 °C

5: 41 percent / 2-hydroxypyridine / 2 h / 120 °C

With 2-hydroxypyridin; hydrogenchloride; aluminium trichloride; thionyl chloride; ammonia; N,N-dimethyl-formamide; In dichloromethane; chloroform; dimethyl sulfoxide;
DOI:10.1021/jm00122a020