5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine

Base Information

• Chemical Name: 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine
• CAS No.: 116700-91-5
• Molecular Formula: C₂₇H₃₇N₇O₅
• Molecular Weight: 539.635
• Mol file: 116700-91-5.mol

Synonyms:5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine

Chemical Property of 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine

There total 3 articles about 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine 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: 47.5%

6-(benzyloxycarbonylamino)-1-iodohexane (51224-11-4) + 5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine (21950-36-7) → 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine (116700-91-5)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 70 ℃; for 18h;

DOI:10.1021/jo00256a010

Reference yield:

N-benzyloxycarbonyl-6-amino-1-hexanol (17996-12-2) → 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine (116700-91-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 63.5 percent

2: 94.6 percent / NaI

3: 47.5 percent / N,N-diisopropylethylamine / acetonitrile / 18 h / 70 °C

With N-ethyl-N,N-diisopropylamine; sodium iodide; In acetonitrile;

DOI:10.1021/jo00256a010

Reference yield:

phenylmethyl <6-<<(4-methylphenyl)sulfonyl>oxy>hexyl>carbamate (51224-12-5) → 5'-<<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>amino>-5'-deoxy-2',3'-O-isopropylideneadenosine (116700-91-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 94.6 percent / NaI

2: 47.5 percent / N,N-diisopropylethylamine / acetonitrile / 18 h / 70 °C

With N-ethyl-N,N-diisopropylamine; sodium iodide; In acetonitrile;

DOI:10.1021/jo00256a010

upstream raw materials:

6-(benzyloxycarbonylamino)-1-iodohexane

5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine

N-benzyloxycarbonyl-6-amino-1-hexanol

phenylmethyl <6-<<(4-methylphenyl)sulfonyl>oxy>hexyl>carbamate

Downstream raw materials:

methyl N⁴-<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>-N⁴-(2',3'-O-isopropylidene-5'-adenosyl)-2(R,S)-(trifluoroacetamido)-4-aminobutyrate

N⁴-<6-<<(phenylmethoxy)carbonyl>amino>-1-hexyl>-N⁴-(2',3'-O-isopropylidene-5'-adenosyl)-2(R,S),4-diaminobutanoic acid