N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

Base Information

Chemical Name:N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide
CAS No.:1607432-62-1
Molecular Formula:C₂₂H₂₁FN₆O₂S
Molecular Weight:452.512
Hs Code.:

Synonyms:N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

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Chemical Property of N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

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Technology Process of N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

There total 9 articles about N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-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:

: 1607432-16-5
N-[5-(5-fluoropyrimidin-2-yl)-6a-(3-pyridyl)-3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-1-carbothioyl]benzamide

: 1607432-62-1
N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

Guidance literature:: With acetic acid; zinc; at 20 ℃; for 2h; Sonication;

Reference yield:

: 17694-68-7
3-(2-bromoacetyl)pyridine hydrobromide

: 1607432-62-1
N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

Guidance literature:: Multi-step reaction with 8 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.67 h / 0 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.67 h / 0 °C

3: triethylamine; titanium(IV) tetraethanolate / toluene / 5 h / 75 °C

4: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

5: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 3 h / 110 °C

6: trifluoroacetic acid / 1 h / 60 °C

7: tetrahydrofuran / 2 h / 0 - 20 °C

8: zinc; acetic acid / 2 h / 20 °C / Sonication

With titanium(IV) tetraethanolate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; zinc; In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene;

Reference yield:

: 350-03-8
methyl-3-pyridylketone

: 1607432-62-1
N-[[1-(5-fluoropyrimidin-2-yl)-4-(hydroxymethyl)-3-(3-pyridyl)pyrrolidin-3-yl]carbamothioyl]benzamide

Guidance literature:: Multi-step reaction with 9 steps

1: hydrogen bromide; bromine / water; acetic acid / 0 - 75 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.67 h / 0 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1.67 h / 0 °C

4: triethylamine; titanium(IV) tetraethanolate / toluene / 5 h / 75 °C

5: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

6: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 3 h / 110 °C

7: trifluoroacetic acid / 1 h / 60 °C

8: tetrahydrofuran / 2 h / 0 - 20 °C

9: zinc; acetic acid / 2 h / 20 °C / Sonication

With titanium(IV) tetraethanolate; hydrogen bromide; bromine; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; zinc; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; acetic acid; toluene;