tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

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Chemical Name:tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate
CAS No.:873581-49-8
Molecular Formula:C₄₆H₅₄N₆O₇S
Molecular Weight:835.037
Hs Code.:

tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

Synonyms:tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

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Chemical Property of tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

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Technology Process of tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

There total 7 articles about tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate 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:

: 873581-47-6
(9H-fluoren-9-yl)methyl (5-amino-4-phenylthiazol-2-yl)carbamate

: 873581-32-9
tert-butyl ((S)-1-(((S)-1-cyclohexyl-2-((S)-2-(fluorocarbonyl)pyrrolidin-1-yl)-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

: 873581-49-8
tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 144h;

Reference yield:

: 912338-14-8
methyl (2S)-2-[(2S)-2-{[(tert-butoxy)carbonyl](methyl)amino}propanamido]-2-cyclohexylacetate

: 873581-49-8
tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: water; lithium hydroxide monohydrate / acetone / 1 h / 0 °C

2: 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; 4-methyl-morpholine / tetrahydrofuran; N,N-dimethyl-formamide / 20 °C

3: water; lithium hydroxide monohydrate / acetone / 1 h / 0 °C

4: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 1 h / 0 °C

5: pyridine / dichloromethane / 1 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; pyridine; trifluoro-[1,3,5]triazine; lithium hydroxide monohydrate; water; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone;

Reference yield:

: 894789-27-6
(2S)-2-[(2S)-2-[[(tert-butoxy)carbonyl](methyl)amino]propanamido]-2-cyclohexylacetic acid

: 873581-49-8
tert-butyl ((S)-1-(((S)-2-((S)-2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylthiazol-5-yl)carbamoyl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)amino)-1-oxopropan-2-yl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; 4-methyl-morpholine / tetrahydrofuran; N,N-dimethyl-formamide / 20 °C

2: water; lithium hydroxide monohydrate / acetone / 1 h / 0 °C

3: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 1 h / 0 °C

4: pyridine / dichloromethane / 1 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; pyridine; trifluoro-[1,3,5]triazine; lithium hydroxide monohydrate; water; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone;