(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

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Chemical Name:(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol
CAS No.:807334-13-0
Molecular Formula:C₁₈H₂₂N₂O₅
Molecular Weight:346.383
Hs Code.:

Synonyms:(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

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Chemical Property of (2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

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Technology Process of (2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

There total 4 articles about (2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol 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: 53.0%

: 438232-16-7
1-methyl-3-[3-(phenyl)-1,2,4-oxadiazol-5-yl]propyl-4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside

: 807334-13-0
(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

: 807334-12-9
(2R,3S,6S)-2-Hydroxymethyl-6-[(R)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: With water; triethylamine; In methanol; at 20 ℃;
DOI:10.1016/j.tet.2004.08.075

Reference yield:

: 2873-29-2
D-glucal triacetate

: 807334-13-0
(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / montmorillonite K-10 / CH₂Cl₂ / Heating

2: 53 percent / Et₃N; H₂O / methanol / 20 °C

With montmorillonite K-10; water; triethylamine; In methanol; dichloromethane; 1: Ferrier's rearrangement;
DOI:10.1016/j.tet.2004.08.075

Reference yield:

: 438232-12-3
4-(3-phenyl-[1,2,4]oxadiazol-5-yl)-butan-2-ol

: 807334-13-0
(2R,3S,6S)-2-Hydroxymethyl-6-[(S)-1-methyl-3-(3-phenyl-[1,2,4]oxadiazol-5-yl)-propoxy]-3,6-dihydro-2H-pyran-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / montmorillonite K-10 / CH₂Cl₂ / Heating

2: 53 percent / Et₃N; H₂O / methanol / 20 °C

With montmorillonite K-10; water; triethylamine; In methanol; dichloromethane; 1: Ferrier's rearrangement;
DOI:10.1016/j.tet.2004.08.075