methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside
CAS No.:273921-13-4
Molecular Formula:C₂₄H₂₉NO₇S
Molecular Weight:475.563
Hs Code.:

Synonyms:methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Suppliers and Price of methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

There total 6 articles about methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside 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: 40.0%

: 110-91-8,99108-56-2
morpholine

: 273921-07-6
methyl 2,3-dideoxy-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-erythro-hex-2-enopyranoside

: 4-((2R,4aR,6S,7R,8R,8aR)-8-Benzenesulfonyl-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-morpholine

: 273921-13-4
methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Guidance literature:: at 80 - 90 ℃; for 24h;
DOI:10.1021/jo991380d

Reference yield:

: 273921-02-1
(2R,4aR,6S,7R,8S,8aR)-6-Methoxy-2-phenyl-8-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

: 273921-13-4
methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / magnesium monoperoxyphthalate / methanol / 2.5 h / 20 °C

2: pyridine / 4 °C

3: 4.12 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 0.08 h

4: 40 percent / 24 h / 80 - 90 °C

With magnesium monoperoxyphthalate hexahydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In pyridine; methanol; dichloromethane; 1: Oxidation / 2: mesylation / 3: Elimination / 4: Addition;
DOI:10.1021/jo991380d

Reference yield:

: 108-98-5
thiophenol

: 273921-13-4
methyl 2,3-dideoxy-2-N-morpholino-4,6-O-(phenylmethylene)-3-C-phenylsulfonyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / 1,1,3,3-tetramethylguanidine / dimethylformamide / 3 h / 80 - 90 °C

2: 100 percent / magnesium monoperoxyphthalate / methanol / 2.5 h / 20 °C

3: pyridine / 4 °C

4: 4.12 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 0.08 h

5: 40 percent / 24 h / 80 - 90 °C

With magnesium monoperoxyphthalate hexahydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N,N,N',N'-tetramethylguanidine; In pyridine; methanol; dichloromethane; N,N-dimethyl-formamide; 1: Addition / 2: Oxidation / 3: mesylation / 4: Elimination / 5: Addition;
DOI:10.1021/jo991380d