N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

Base Information

Chemical Name:N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide
CAS No.:1391001-93-6
Molecular Formula:C₂₀H₂₀F₂N₂O₃S
Molecular Weight:406.453
Hs Code.:

Synonyms:N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

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Chemical Property of N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

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Technology Process of N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

There total 6 articles about N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)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: 75.0%

: 1391001-92-5
((2S,3R,4S)-4-amino-2-(fluoromethyl)-4-(2-fluorophenyl)tetrahydrofuran-3-yl)methanol

: 532-55-8
Benzoyl isothiocyanate

: 1391001-93-6
N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

Guidance literature:: In dichloromethane; at 0 - 20 ℃; for 18h;

Reference yield: 75.0%

: 1391001-93-6
N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

Guidance literature:: In hexane;

Reference yield:

: 1391001-87-8
tert-butyl (S)-2-((1-fluorobut-3-en-2-yl)oxy)acetate

: 1391001-93-6
N-(((3S,4R,5S)-5-(fluoromethyl)-3-(2-fluorophenyl)-4-(hydroxymethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: formic acid / 0 - 20 °C

2.1: 1,1'-carbonyldiimidazole / dichloromethane / 3 - 20 °C

2.2: 3 - 20 °C

3.1: n-butyllithium / hexane; tetrahydrofuran / -78 - -60 °C / Inert atmosphere

3.2: -78 - -60 °C

4.1: hydroxylamine hydrochloride; sodium acetate / methanol / 1.5 h / 50 °C

5.1: hydroquinone / xylene / 5 h / Reflux

6.1: zinc; acetic acid / 0 - 20 °C

7.1: dichloromethane / 18 h / 0 - 20 °C

With n-butyllithium; formic acid; hydroxylamine hydrochloride; sodium acetate; acetic acid; hydroquinone; 1,1'-carbonyldiimidazole; zinc; In tetrahydrofuran; methanol; hexane; dichloromethane; xylene;