D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)

Base Information

Chemical Name:D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)
CAS No.:73352-73-5
Molecular Formula:C22H43 N5 O12
Molecular Weight:569.61
Hs Code.:

D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)

Synonyms:Sch24628

Suppliers and Price of D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)

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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 D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)

Chemical Property:

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI)

There total 6 articles about D-Streptamine,O-6-amino-6-deoxy-a-D-glucopyranosyl-(1®4)-O-[3-deoxy-4-C-methyl-3-(methylamino)-b-L-arabinopyranosyl-(1®6)]-N1-[(2-aminoethoxy)carbonyl]-2-deoxy- (9CI) 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: 82.0%

: 73352-63-3
3,6',3''-tris-N-benzyloxycarbonyl-1-N-(2-benzyloxycarbonylaminoethoxycarbonyl)gentamicin B

: 73352-73-5
1-N-(2-aminoethoxycarbonyl)gentamicin B

Guidance literature:: With hydrogen; palladium - carbon; In methanol; at 25 ℃; for 18h; Pressure (range begins): 55 ;
DOI:10.1039/P19810002186

Reference yield:

: 73362-90-0
3,6'-bis-N-benzyloxycarbonyl-1-N-(2-benzyloxycarbonylaminoethoxycarbonyl)gentamicin B

: 73352-73-5
1-N-(2-aminoethoxycarbonyl)gentamicin B

Guidance literature:: With hydrogenchloride; hydrogen; palladium - carbon; In methanol; at 25 ℃; for 18h; Pressure (range begins): 55 ;
DOI:10.1039/P19810002186

Reference yield:

: 66567-23-5
3,6'-bis-N-benzyloxycarbonylgentamicin B

: 73352-73-5
1-N-(2-aminoethoxycarbonyl)gentamicin B

Guidance literature:: Multi-step reaction with 5 steps

1: 62 percent / dimethylformamide / 2 h / 25 °C

2: 93 percent / sodium carbonate / acetone; H₂O / 18 h / 25 °C

3: 57 percent / acetic acid, zinc / H₂O / 48 h / 25 °C

4: 78 percent / triethylamine / dimethylformamide / 3 h / 25 °C

5: 82 percent / hydrogen / 10percent palladium - carbon / methanol / 18 h / 25 °C

With hydrogen; sodium carbonate; acetic acid; triethylamine; zinc; palladium - carbon; In methanol; water; N,N-dimethyl-formamide; acetone;
DOI:10.1039/P19810002186