(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

Base Information

Chemical Name:(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester
CAS No.:156143-57-6
Molecular Formula:C₄₀H₆₀N₂O₈S₂
Molecular Weight:761.057
Hs Code.:

(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

Synonyms:(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

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Chemical Property of (4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

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Technology Process of (4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

There total 7 articles about (4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic 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:

: 77292-91-2
α-(4-bromomethylphenyl)acetic acid tert-butyl ester

: 156143-57-6
(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 53 percent / KI, benzyltrimethylammonium hydroxide / dioxane; H₂O / 3 h / Ambient temperature

2: 72 percent / 1 N aq. HCl / diethyl ether / 4 h / Ambient temperature

3: 97 percent / dimethylformamide

4: 50 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

5: pyridine, KOH / 4 °C

6: dimethylformamide / Ambient temperature

7: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With pyridine; hydrogenchloride; potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; iodine; N-benzyl-trimethylammonium hydroxide; potassium iodide; In 1,4-dioxane; diethyl ether; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014

Reference yield:

: 156143-53-2
2-Amino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propionic acid ethyl ester

: 156143-57-6
(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / dimethylformamide

2: 50 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

3: pyridine, KOH / 4 °C

4: dimethylformamide / Ambient temperature

5: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With pyridine; potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; iodine; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014

Reference yield:

: 156143-55-4
[4-(2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-phenyl]-acetic acid tert-butyl ester

: 156143-57-6
(4-{2-tert-Butoxycarbonylamino-3-[2-tert-butoxycarbonylamino-3-(4-tert-butoxycarbonylmethyl-phenyl)-propyldisulfanyl]-propyl}-phenyl)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine, KOH / 4 °C

2: dimethylformamide / Ambient temperature

3: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With pyridine; potassium hydroxide; sodium hydroxide; iodine; In N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014