{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester
CAS No.:76381-75-4
Molecular Formula:C₂₈H₃₇BrN₈O₇
Molecular Weight:677.555
Hs Code.:

{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

Synonyms:{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

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Chemical Property of {(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

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Technology Process of {(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

There total 5 articles about {(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic 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:

: 1070-19-5
N-(tert-butyloxycarbonyl) azide

: 76381-75-4
{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 44 percent / magnesium hydroxide / H₂O; dioxane / 20 h / 40 °C

2: 70.5 percent / N-hydroxysuccinimide, dicyclohexylcarbodiimide / dimethylformamide / 20 h / Ambient temperature

3: 88.3 percent / H₂, glacial CH₃COOH / 10percent Pd/C / 4 h / 760 Torr / Ambient temperature

4: 2.) 1percent NH₄OH / 1.) dioxane, RT, 3 d, 2.) methanol

With magnesium hydroxide; ammonium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; hydrogen; acetic acid; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00135a013

Reference yield:

: 949-99-5
4-nitro-3-phenyl-L-alanine

: 76381-75-4
{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 44 percent / magnesium hydroxide / H₂O; dioxane / 20 h / 40 °C

2: 70.5 percent / N-hydroxysuccinimide, dicyclohexylcarbodiimide / dimethylformamide / 20 h / Ambient temperature

3: 88.3 percent / H₂, glacial CH₃COOH / 10percent Pd/C / 4 h / 760 Torr / Ambient temperature

4: 2.) 1percent NH₄OH / 1.) dioxane, RT, 3 d, 2.) methanol

With magnesium hydroxide; ammonium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; hydrogen; acetic acid; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00135a013

Reference yield:

: 33305-77-0
Boc-Phe(p-NO₂)-OH

: 76381-75-4
{(S)-2-[4-(2-Bromo-acetylamino)-phenyl]-1-[(2S,3S,4R,5R)-5-(6-dimethylamino-purin-9-yl)-4-hydroxy-2-hydroxymethyl-tetrahydro-furan-3-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 70.5 percent / N-hydroxysuccinimide, dicyclohexylcarbodiimide / dimethylformamide / 20 h / Ambient temperature

2: 88.3 percent / H₂, glacial CH₃COOH / 10percent Pd/C / 4 h / 760 Torr / Ambient temperature

3: 2.) 1percent NH₄OH / 1.) dioxane, RT, 3 d, 2.) methanol

With ammonium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; hydrogen; acetic acid; dicyclohexyl-carbodiimide; palladium on activated charcoal; In N,N-dimethyl-formamide;
DOI:10.1021/jm00135a013