3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

Base Information

Chemical Name:3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose
CAS No.:148404-67-5
Molecular Formula:C₂₀H₂₇NO₇
Molecular Weight:393.437
Hs Code.:

Synonyms:3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

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Chemical Property of 3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

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Technology Process of 3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

There total 4 articles about 3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose 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: 85.0%

: 148404-66-4
3-benzyloxycarbonylaminopropyl 2,3-O-isopropylidene-α-L-rhamnopyranoside

: 148404-67-5
3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

Guidance literature:: With 4 A molecular sieve; 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate; In 1,2-dichloro-ethane; at 20 ℃; for 0.166667h;
DOI:10.1016/0008-6215(93)80102-K

Reference yield:

: 34637-22-4
3-[(N-benzyloxycarbonyl)amino]propanol

: 148404-67-5
3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / N-iodosuccinimide, 4 Angstroem molecular sieves / trifluoromethanesulfonic acid / 1,2-dichloro-ethane; diethyl ether / 0.25 h / 0 °C

2: t-BuOK / methanol / 2 h / 20 °C

3: camphorsulfonic acid / acetone / 2 h / 20 °C

4: 85 percent / 4-methylmorpholine N-oxide, 4 Angstroem molecular sieves / tetrapropylammonium per-ruthenate / 1,2-dichloro-ethane / 0.17 h / 20 °C

With N-iodo-succinimide; 4 A molecular sieve; camphor-10-sulfonic acid; potassium tert-butylate; 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate; trifluorormethanesulfonic acid; In methanol; diethyl ether; 1,2-dichloro-ethane; acetone;
DOI:10.1016/0008-6215(93)80102-K

Reference yield:

: 148404-74-4
ethyl 2,3,4-tri-O-benzoyl-1-thio-α-L-rhamnopyranoside

: 148404-67-5
3-benzyloxycarbonylaminopropyl 6-deoxy-2,3-O-isopropylidene-α-L-lyxo-hexopyranosid-4-ulose

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / N-iodosuccinimide, 4 Angstroem molecular sieves / trifluoromethanesulfonic acid / 1,2-dichloro-ethane; diethyl ether / 0.25 h / 0 °C

2: t-BuOK / methanol / 2 h / 20 °C

3: camphorsulfonic acid / acetone / 2 h / 20 °C

4: 85 percent / 4-methylmorpholine N-oxide, 4 Angstroem molecular sieves / tetrapropylammonium per-ruthenate / 1,2-dichloro-ethane / 0.17 h / 20 °C

With N-iodo-succinimide; 4 A molecular sieve; camphor-10-sulfonic acid; potassium tert-butylate; 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate; trifluorormethanesulfonic acid; In methanol; diethyl ether; 1,2-dichloro-ethane; acetone;
DOI:10.1016/0008-6215(93)80102-K