Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester
CAS No.:474409-88-6
Molecular Formula:C₃₂H₃₁N₅O₉SSe
Molecular Weight:740.652
Hs Code.:

Synonyms:Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

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Chemical Property of Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

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Technology Process of Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

There total 4 articles about Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl 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: 96.0%

: 108-24-7
acetic anhydride

: 474409-86-4
Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-2-ylmethyl ester

: 474409-88-6
Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

Guidance literature:: Acetic acid (2R,3R,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-2-ylmethyl ester; With 3-chloro-benzenecarboperoxoic acid; at -70 ℃;

acetic anhydride; In dichloromethane; at 20 ℃;
DOI:10.1016/S0040-4039(02)01131-0

Reference yield:

: 209048-61-3
1,4-anhydro-2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-diyl)-4-thio-D-erythro-pent-1-enitol

: 474409-88-6
Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: LDA

1.2: 69 percent / NaBH₄

2.1: 40 percent / acetonitrile; CH₂Cl₂ / -40 °C

3.1: Bu₄NF / tetrahydrofuran

3.2: 90 percent / iPr₂NEt; DMAP / CH₂Cl₂

4.1: m-CPBA / -70 °C

4.2: 96 percent / CH₂Cl₂ / 20 °C

With tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane; acetonitrile; 4.2: seleno-Pummerer reaction;
DOI:10.1016/S0040-4039(02)01131-0

Reference yield:

: 474409-49-9
1,4-anhydro-1-(tert-butyldimethylsilyloxymethyl)-2-deoxy-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-thio-D-erythropento-1-enitol

: 474409-88-6
Acetic acid (2R,4R,5R)-4-acetoxy-2,5-bis-acetoxymethyl-2-(6-benzoylamino-purin-9-yl)-3-phenylselanyl-tetrahydro-thiophen-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 40 percent / acetonitrile; CH₂Cl₂ / -40 °C

2.1: Bu₄NF / tetrahydrofuran

2.2: 90 percent / iPr₂NEt; DMAP / CH₂Cl₂

3.1: m-CPBA / -70 °C

3.2: 96 percent / CH₂Cl₂ / 20 °C

With tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; acetonitrile; 3.2: seleno-Pummerer reaction;
DOI:10.1016/S0040-4039(02)01131-0