methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside

Base Information

• Chemical Name: methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside
• CAS No.: 136029-20-4
• Molecular Formula: C₁₈H₂₃NO₆S
• Molecular Weight: 381.45
• Mol file: 136029-20-4.mol

Synonyms:methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside

Chemical Property of methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside

There total 7 articles about methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside 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: 32.0%

methanol (67-56-1) + (3S,4R,5S,6R)-3-O-benzyl-3,4,5,6,7-pentahydroxy-4,5:6,7-di-O-isopropylidene-1-(2-thiazolyl)-1-hexanone → methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside (136029-20-4)

Guidance literature:

With hydrogenchloride; at 0 ℃; for 2h;

Reference yield: 25.0%

methanol (67-56-1) + (S)-3-Benzyloxy-3-((4R,5R,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-1-thiazol-2-yl-propan-1-one (136029-19-1) → methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside (136029-20-4)

Guidance literature:

With hydrogenchloride; at 0 ℃; for 2h;

DOI:10.1016/S0040-4039(00)79735-8

Reference yield:

2-bromo-1-thiazol-2-yl-ethanone (3292-77-1) → methyl 3-O-benzyl-2-deoxy-1-(2-thiazolyl)-α-D-gluco-heptopyranoside (136029-20-4)

Guidance literature:

Multi-step reaction with 5 steps

1: 95 percent / toluene / 3 h / Ambient temperature

2: 95 percent / 1N aq. NaOH / 0.5 h

3: 88 percent / CHCl₃ / 24 h / 25 °C

4: 82 percent / tetrahydrofuran / 5 h / -50 °C

5: 32 percent / HCl / 2 h / 0 °C

With hydrogenchloride; sodium hydroxide; In tetrahydrofuran; chloroform; toluene;

upstream raw materials:

methanol

(S)-3-Benzyloxy-3-((4R,5R,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-1-thiazol-2-yl-propan-1-one

2-bromo-1-thiazol-2-yl-ethanone

1-(thiazol-2-yl)-2-(triphenyl-λ ⁵-phosphanylidene)ethan-1-one