2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

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Chemical Name:2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester
CAS No.:473710-46-2
Molecular Formula:C₄₂H₇₃N₅O₁₁Si₂
Molecular Weight:880.24
Hs Code.:

2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(<i>tert</i>-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2<i>H</i>-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid <i>tert</i>-butyl ester

Synonyms:2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

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Chemical Property of 2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

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Technology Process of 2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

There total 7 articles about 2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-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: 97.0%

: 473710-45-1
2-[3-(2-benzyloxycarbonylamino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

: 473710-46-2
2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; atmospheric pressure;
DOI:10.1016/S0960-894X(03)00671-1

Reference yield:

: 94226-56-9
tert-butyl 2-(dibenzylamino)ethanoate

: 473710-46-2
2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: LDA / tetrahydrofuran / 1 h / -78 °C

1.2: 31 percent / tetrahydrofuran / 17 h / -78 - -35 °C

2.1: H₂ / 10 percent Pd/C / methanol

3.1: 54 percent / NaBH(OAc)3; AcOH / tetrahydrofuran / 4 h / 20 °C

4.1: 97 percent / H₂ / 10 percent Pd/C / methanol / 20 °C / atmospheric pressure

With hydrogen; sodium tris(acetoxy)borohydride; acetic acid; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1016/S0960-894X(03)00671-1

Reference yield:

: 137233-53-5
2',3'-O-bis(tert-butyldimethylsilyl)-3-N-(p-methoxybenzyl)uridine-5'-aldehyde

: 473710-46-2
2-[3-(2-amino-3-hydroxy-butyrylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: LDA / tetrahydrofuran / 1 h / -78 °C

1.2: 31 percent / tetrahydrofuran / 17 h / -78 - -35 °C

2.1: H₂ / 10 percent Pd/C / methanol

3.1: 54 percent / NaBH(OAc)3; AcOH / tetrahydrofuran / 4 h / 20 °C

4.1: 97 percent / H₂ / 10 percent Pd/C / methanol / 20 °C / atmospheric pressure

With hydrogen; sodium tris(acetoxy)borohydride; acetic acid; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1016/S0960-894X(03)00671-1