3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

Base Information

Chemical Name:3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid
CAS No.:1220870-49-4
Molecular Formula:C₂₃H₂₅FN₄O₃S
Molecular Weight:456.541
Hs Code.:

Synonyms:3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

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Chemical Property of 3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

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Technology Process of 3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

There total 8 articles about 3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid 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: 66.0%

: 1220708-88-2
N-butyl-2-fluoro-N-(5-(4-formylphenyl)-1,3,4-thiadiazol-2-yl)benzamide

: 107-95-9
3-amino propanoic acid

: 1220870-49-4
3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

Guidance literature:: N-butyl-2-fluoro-N-(5-(4-formylphenyl)-1,3,4-thiadiazol-2-yl)benzamide; 3-amino propanoic acid; With acetic acid; In methanol; at 20 ℃; for 1h;

With methanol; sodium cyanoborohydride; for 6h;

Reference yield: 28.0%

: 1220870-49-4
3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

Guidance literature:

Reference yield:

: 592-82-5
butyl isothiocyanate

: 1220870-49-4
3-(4-(5-(N-butyl-2-fluorobenzamido)-1,3,4-thiadiazol-2-yl)benzylamino)propanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrazine hydrate / methanol / 10 - 15 °C

2.1: trichlorophosphate / 1,4-dioxane / 0.5 h / 20 °C

2.2: 80 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -60 - 20 °C / Inert atmosphere

5.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.17 h / 20 °C

5.2: 2 h / 60 °C

6.1: acetic acid / methanol / 1 h / 20 °C

6.2: 6 h

With dmap; lithium aluminium tetrahydride; oxalyl dichloride; hydrazine hydrate; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;