(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

Base Information

Chemical Name:(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester
CAS No.:1054640-35-5
Molecular Formula:C₃₇H₄₁NO₇S
Molecular Weight:643.801
Hs Code.:

(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

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Chemical Property of (S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

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Technology Process of (S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

There total 4 articles about (S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-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:

: (2S,3S,4R)-2-(1-Hydroxy-1-methyl-ethyl)-3,4-dihydro-2H-pyran-3,4-diol

: 1054640-35-5
(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: NaH; Bu₄NI / tetrahydrofuran / 20 °C

2: Ph₃P*HBr / CH₂Cl₂ / 20 °C

3: NaOH / tetrahydrofuran; H₂O / 0 - 20 °C

4: triethylamine; 4-(dimethylamino)pyridine; N-ethyldiisopropylamine / tetrahydrofuran

With dmap; sodium hydroxide; triphenylphosphine hydrobromide; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo010880f

Reference yield:

: 249757-75-3
1,5-anhydro-2,7-dideoxy-6-C-methyl-3,4,6-tris-O-(phenylmethyl)-D-arabino-hept-1-enitol

: 1054640-35-5
(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Ph₃P*HBr / CH₂Cl₂ / 20 °C

2: NaOH / tetrahydrofuran; H₂O / 0 - 20 °C

3: triethylamine; 4-(dimethylamino)pyridine; N-ethyldiisopropylamine / tetrahydrofuran

With dmap; sodium hydroxide; triphenylphosphine hydrobromide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo010880f

Reference yield:

: 249757-80-0
(2S)-[[2,7-dideoxy-6-C-methyl-3,4,6-tris-O-(phenylmethyl)-α-D-arabino-heptopyranosyl]oxy]propanoic acid ethyl ester

: 1054640-35-5
(S)-2-[(2R,4R,5S,6S)-4,5-Bis-benzyloxy-6-(1-benzyloxy-1-methyl-ethyl)-tetrahydro-pyran-2-yloxy]-propionic acid 2-thioxo-2H-pyridin-1-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaOH / tetrahydrofuran; H₂O / 0 - 20 °C

2: triethylamine; 4-(dimethylamino)pyridine; N-ethyldiisopropylamine / tetrahydrofuran

With dmap; sodium hydroxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; water;
DOI:10.1021/jo010880f