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

Base Information

Chemical Name:2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester
CAS No.:232918-66-0
Molecular Formula:C₂₇H₃₄ClN₅O₆S
Molecular Weight:592.116
Hs Code.:

2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid <i>tert</i>-butyl ester

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Chemical Property of 2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

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Technology Process of 2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

There total 7 articles about 2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester 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:

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

: 232918-66-0
2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 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

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

Reference yield:

: 619-66-9
4-Carboxybenzaldehyde

: 232918-66-0
2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 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

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

Reference yield:

: 77215-55-5
tert-butyl 2-N-carbobenzoxy-(S)-2,3-diaminopropionate

: 232918-66-0
2-(4-chloro-benzenesulfonylamino)-3-{4-[2-(1,4,5,6-tetrahydro-pyrimidin-2-ylcarbamoyl)-ethyl]-benzoylamino}-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / TOTU; ethyldiisopropylamine / dimethylformamide / 7 h / 20 °C

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

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

4: dimethylformamide / 8 h / 20 °C

With O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;