(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

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Chemical Name:(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate
CAS No.:1443792-05-9
Molecular Formula:C₃₆H₄₃N₃O₄S
Molecular Weight:613.821
Hs Code.:

Synonyms:(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

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Chemical Property of (S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

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Technology Process of (S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

There total 8 articles about (S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate 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: 29.0%

: 1443791-90-9
(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(2-(4-(heptyloxy)benzoyl)hydrazine-carbonyl)phenyl)propanoate

: 1443792-05-9
(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

Guidance literature:: With Lawessons reagent; In tetrahydrofuran; at 65 ℃; for 1h;

Reference yield:

: 15872-42-1
4-heptyloxybenzoic acid

: 1443792-05-9
(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 1,1'-carbonyldiimidazole; hydrazine hydrate / tetrahydrofuran / 4 h / 20 °C

2: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 2 h / 20 °C

3: Lawessons reagent / tetrahydrofuran / 1 h / 65 °C

With Lawessons reagent; 4-methyl-morpholine; hydrazine hydrate; 1,1'-carbonyldiimidazole; isobutyl chloroformate; In tetrahydrofuran;

Reference yield:

: 1443791-81-8
(S)-methyl 4-(2-(4-(tert-butyl)benzamido)-3-methoxy-3-oxopropyl)benzoate

: 1443792-05-9
(S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-(5-(4-(heptyloxy)phenyl)-1,3,4-thiadiazol-2-yl)phenyl)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hydroxide monohydrate; water / 2 h / 0 °C

1.2: pH 7

2.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 2 h / 20 °C

3.1: Lawessons reagent / tetrahydrofuran / 1 h / 65 °C

With Lawessons reagent; 4-methyl-morpholine; lithium hydroxide monohydrate; water; isobutyl chloroformate; In tetrahydrofuran;