4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

Base Information

Chemical Name:4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione
CAS No.:960503-86-0
Molecular Formula:C₁₄H₈BrFN₂S₃
Molecular Weight:399.331
Hs Code.:

Synonyms:4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

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Chemical Property of 4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

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Technology Process of 4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

There total 5 articles about 4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione 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: 95.0%

: 75-15-0,12122-00-8
carbon disulfide

: 960503-85-9
4-[(3-bromophenyl)(isothiocyanato)methyl]-3-fluoropyridine

: 960503-86-0
4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at -78 - 20 ℃; for 0.5h;

Reference yield:

: 960503-84-8
1-(3-bromophenyl)-1-(3-fluoropyridin-4-yl)methanamine

: 960503-86-0
4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 2 h / 25 °C

2: potassium tert-butylate / tetrahydrofuran / 0.5 h / -78 - 20 °C

With potassium tert-butylate; In tetrahydrofuran; dichloromethane;

Reference yield:

: (R)-N-[(1E)-(3-bromophenyl)methylidene]-2-methylpropane-2-sulfinamide

: 960503-86-0
4-(3-Bromophenyl)-4-(3-fluoropyridin-4-yl)-1,3-thiazolidine-2,5-dithione

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C

1.2: 0.08 h / -78 °C

2.1: hydrogenchloride; methanol / diethyl ether / 0.17 h

3.1: dichloromethane / 2 h / 25 °C

4.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / -78 - 20 °C

With hydrogenchloride; methanol; potassium tert-butylate; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane;