Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

Base Information

Chemical Name:Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester
CAS No.:200335-33-7
Molecular Formula:C₃₁H₃₆N₂O₇
Molecular Weight:548.636
Hs Code.:

Synonyms:Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

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Chemical Property of Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

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Technology Process of Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

There total 5 articles about Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-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:

: 187342-10-5
5-deoxy-5-isopropylamino-1,2-O-isopropylidene-α-D-xylofuranose

: 200335-33-7
Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / NaH, NaI / tetrahydrofuran / 1.) 0 deg C, 6 h, 2.) room temperature, overnight

2: 85 percent / KHCO₃ / tetrahydrofuran; H₂O / 1.5 h / Ambient temperature

3: 53 percent / I₂ / methanol / 4 h / Heating

4: 1.) Py, 0 deg C, 1 h, 2.) 0 deg C, 1 h; room temperature, 12 h

With iodine; sodium hydride; potassium hydrogencarbonate; sodium iodide; In tetrahydrofuran; methanol; water;
DOI:10.1016/S0040-4020(97)10173-9

Reference yield:

: 200335-29-1
3-O-benzyl-5-deoxy-5-isopropylamino-1,2-O-isopropylidenexylofuranose

: 200335-33-7
Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / KHCO₃ / tetrahydrofuran; H₂O / 1.5 h / Ambient temperature

2: 53 percent / I₂ / methanol / 4 h / Heating

3: 1.) Py, 0 deg C, 1 h, 2.) 0 deg C, 1 h; room temperature, 12 h

With iodine; potassium hydrogencarbonate; In tetrahydrofuran; methanol; water;
DOI:10.1016/S0040-4020(97)10173-9

Reference yield:

: 200335-30-4
((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl)-isopropyl-carbamic acid benzyl ester

: 200335-33-7
Phenyl-carbamic acid (2S,3R,4S,5R)-4-benzyloxy-5-[(benzyloxycarbonyl-isopropyl-amino)-methyl]-2-methoxy-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / I₂ / methanol / 4 h / Heating

2: 1.) Py, 0 deg C, 1 h, 2.) 0 deg C, 1 h; room temperature, 12 h

With iodine; In methanol;
DOI:10.1016/S0040-4020(97)10173-9