(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

Base Information

Chemical Name:(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol
CAS No.:282101-81-9
Molecular Formula:C₁₁H₂₁NO₆
Molecular Weight:263.291
Hs Code.:

Synonyms:(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

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Chemical Property of (1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

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Technology Process of (1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

There total 5 articles about (1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol 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: 100.0%

: 282101-80-8
(1S,2R,3R,6S)-6-Azido-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

: 282101-81-9
(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

Guidance literature:: With hydrogen; nickel; In 1,4-dioxane; water; at 20 ℃; for 3h;
DOI:10.7164/antibiotics.53.430

Reference yield:

: 282101-79-5
(1R,2S,3R,6R)-6-Methoxymethoxy-5-methoxymethoxymethyl-cyclohex-4-ene-1,2,3-triol

: 282101-81-9
(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / HN₃; Ph₃P; DEAD / tetrahydrofuran / 1 h / 20 °C

2: 100 percent / H₂ / Raney Ni / H₂O; dioxane / 3 h / 20 °C

With tris-(2-chloro-ethyl)-amine; hydrogen; triphenylphosphine; diethylazodicarboxylate; nickel; In tetrahydrofuran; 1,4-dioxane; water; 1: Substitution / 2: Hydrogenation;
DOI:10.7164/antibiotics.53.430

Reference yield:

: 282101-77-3
(4R,5S,6R)-4,5,6-Tris-(tert-butyl-dimethyl-silanyloxy)-2-hydroxymethyl-cyclohex-2-enone

: 282101-81-9
(1S,2R,3R,6S)-6-Amino-3-methoxymethoxy-4-methoxymethoxymethyl-cyclohex-4-ene-1,2-diol

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / Zn(BH₄)2 / diethyl ether / 1 h / 0 °C

2: 85 percent / n-Bu₄NI; DIPEA / 1,2-dichloro-ethane / 24 h / 50 °C

3: 97 percent / tetrabutylammonium fluoride (TBAF) / tetrahydrofuran / 3 h / 20 °C

4: 81 percent / HN₃; Ph₃P; DEAD / tetrahydrofuran / 1 h / 20 °C

5: 100 percent / H₂ / Raney Ni / H₂O; dioxane / 3 h / 20 °C

With zinc(II) tetrahydroborate; tris-(2-chloro-ethyl)-amine; tetrabutyl ammonium fluoride; hydrogen; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; nickel; In tetrahydrofuran; 1,4-dioxane; diethyl ether; water; 1,2-dichloro-ethane; 1: Reduction / 2: Substitution / 3: deprotection / 4: Substitution / 5: Hydrogenation;
DOI:10.7164/antibiotics.53.430