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2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane

Base Information
  • Chemical Name:2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane
  • CAS No.:186091-02-1
  • Molecular Formula:C41H40N2O11S
  • Molecular Weight:768.841
  • Hs Code.:
2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane

Synonyms:2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane

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Chemical Property of 2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane
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Technology Process of 2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane

There total 10 articles about 2-azi-1-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyloxy)-6-oxa-8-thianonane 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:
Guidance literature:
Multi-step reaction with 9 steps
1: 95 percent / NaH, Bu4NI / dimethylformamide / 3 h / Ambient temperature
2: 94 percent / aq. acetic acid / Ambient temperature
3: 88 percent / 4-dimethylaminopyridine / pyridine / 48 h / Ambient temperature
4: 84 percent / PCC / pyridine; CH2Cl2 / 96 h
5: 77 percent / aq. acetic acid / 2 h / Ambient temperature
6: 1.) hydroxylamine-O-sulfonic acid, NH3, 2.) Et3N, I2 / 1.) MeOH, -20 deg C, 2 h, 2.) MeOH, 0 deg C, 20 min
7: 1.) tetramethylurea, silver trifluoromethanesulfonate, 4A molecular sieves / 1.) CH2Cl2, rt, 1 h, 2.) CH2Cl2, -20 deg C, 4 h
8: 81 percent / N-bromosucinimide, CaCO3, Br2 / CCl4; H2O / 3 h / Ambient temperature
9: 89 percent / benzoyl peroxide / acetonitrile / 3 h / 0 °C
With dmap; N-Bromosuccinimide; 4 A molecular sieve; ammonia; bromine; iodine; silver trifluoromethanesulfonate; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; pyridinium chlorochromate; tetramethylurea; calcium carbonate; hydroxylamine-O-sulfonic acid; dibenzoyl peroxide; In pyridine; tetrachloromethane; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0008-6215(96)00207-8
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) tetramethylurea, silver trifluoromethanesulfonate, 4A molecular sieves / 1.) CH2Cl2, rt, 1 h, 2.) CH2Cl2, -20 deg C, 4 h
2: 81 percent / N-bromosucinimide, CaCO3, Br2 / CCl4; H2O / 3 h / Ambient temperature
3: 89 percent / benzoyl peroxide / acetonitrile / 3 h / 0 °C
With N-Bromosuccinimide; 4 A molecular sieve; bromine; silver trifluoromethanesulfonate; tetramethylurea; calcium carbonate; dibenzoyl peroxide; In tetrachloromethane; water; acetonitrile;
DOI:10.1016/S0008-6215(96)00207-8
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