{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

Base Information

Chemical Name:{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester
CAS No.:157487-67-7
Molecular Formula:C₄₁H₅₃N₉O₁₁
Molecular Weight:847.926
Hs Code.:

{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

Synonyms:{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

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Chemical Property of {(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

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Technology Process of {(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

There total 9 articles about {(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl 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: 99.5%

: 157487-64-4
[2-(2-{2-[2-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexanoylamino)-5-phenoxymethyl-benzoylamino]-acetylamino}-acetylamino)-acetylamino]-acetic acid ethyl ester

: 157487-67-7
{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

Guidance literature:: With hydrazine hydrate; In methanol; Ambient temperature;

Reference yield:

: 3113-72-2
5-methyl-2-nitrobenzoic acid

: 157487-67-7
{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 32.6 g / AcCl / Heating

2: NBS, benzoyl-peroxide / CCl₄ / Heating

3: aq. NaOH, aliquat / CH₂Cl₂ / 5 h / Ambient temperature

4: 85 percent / aq. 4N KOH / methanol / 2 h / Ambient temperature

5: SOCl₂, DMF / 2 h / Ambient temperature

6: 89 percent / Et₃N / dimethylformamide / 1.) 0 deg C, 2 h; 2.) r.t.

7: H₂ / PtO₂ / methanol; dimethylformamide / 2 h / Ambient temperature

8: DCC / CH₂Cl₂; dimethylformamide / 1.) from -10 deg C to 0 deg C, 2 h; 2.) r.t.

9: 99.5 percent / NH₂NH₂*H₂O / methanol / Ambient temperature

With potassium hydroxide; sodium hydroxide; N-Bromosuccinimide; thionyl chloride; Perbenzoic acid; Aliquat; hydrogen; hydrazine hydrate; triethylamine; acetyl chloride; N,N-dimethyl-formamide; dicyclohexyl-carbodiimide; platinum(IV) oxide; In methanol; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 20587-30-8
5-methyl-2-nitro-benzoic acid methyl ester

: 157487-67-7
{(S)-5-tert-Butoxycarbonylamino-5-[2-({[({[(hydrazinocarbonylmethyl-carbamoyl)-methyl]-carbamoyl}-methyl)-carbamoyl]-methyl}-carbamoyl)-4-phenoxymethyl-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: NBS, benzoyl-peroxide / CCl₄ / Heating

2: aq. NaOH, aliquat / CH₂Cl₂ / 5 h / Ambient temperature

3: 85 percent / aq. 4N KOH / methanol / 2 h / Ambient temperature

4: SOCl₂, DMF / 2 h / Ambient temperature

5: 89 percent / Et₃N / dimethylformamide / 1.) 0 deg C, 2 h; 2.) r.t.

6: H₂ / PtO₂ / methanol; dimethylformamide / 2 h / Ambient temperature

7: DCC / CH₂Cl₂; dimethylformamide / 1.) from -10 deg C to 0 deg C, 2 h; 2.) r.t.

8: 99.5 percent / NH₂NH₂*H₂O / methanol / Ambient temperature

With potassium hydroxide; sodium hydroxide; N-Bromosuccinimide; thionyl chloride; Perbenzoic acid; Aliquat; hydrogen; hydrazine hydrate; triethylamine; N,N-dimethyl-formamide; dicyclohexyl-carbodiimide; platinum(IV) oxide; In methanol; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide;