(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

Base Information

Chemical Name:(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid
CAS No.:232918-11-5
Molecular Formula:C₂₇H₃₅N₅O₆S
Molecular Weight:557.671
Hs Code.:

Synonyms:(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

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Chemical Property of (2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

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Technology Process of (2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

There total 7 articles about (2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic 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:

: 232918-50-2
2-(4-tert-butyl-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

: 232918-11-5
(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃;

Reference yield:

: 228572-45-0
(1,1-dimethylethyl) N-[(phenylmethoxy)carbonyl]-3-[[4-(3-methoxy-3-oxo-propyl)benzoyl]amino]-L-alaninate

: 232918-11-5
(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen; acetic acid / Pd/C / methanol / 7 h / 20 °C

2: triethylamine / dimethylformamide / 4 h / 20 °C

3: dimethylformamide / 8 h / 20 °C

4: trifluoroacetic acid / CH₂Cl₂ / 20 °C

With hydrogen; acetic acid; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 619-66-9
4-Carboxybenzaldehyde

: 232918-11-5
(2S)-2-(4-tert-butyl-benzenesulfonylamino)-3-(4-(2-(1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl)-ethyl)-benzoylamino)-propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 52 percent / piperidine; pyridine / 3 h / Heating

2: 99 percent / hydrogen / Pd/C / dioxane / 7 h / 20 °C

3: 93 percent / TOTU; ethyldiisopropylamine / dimethylformamide / 7 h / 20 °C

4: hydrogen; acetic acid / Pd/C / methanol / 7 h / 20 °C

5: triethylamine / dimethylformamide / 4 h / 20 °C

6: dimethylformamide / 8 h / 20 °C

7: trifluoroacetic acid / CH₂Cl₂ / 20 °C

With piperidine; pyridine; O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; 1: Knoevenagel reaction;