1-(3-o-Acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione

Base Information

• Chemical Name: 1-(3-o-Acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione
• CAS No.: 23583-46-2
• Molecular Formula: C31H30 N2 O6
• Molecular Weight: 526.589
• NSC Number: 76353
• DSSTox Substance ID: DTXSID90291546,DTXSID10946384
• Mol file: 23583-46-2.mol

Synonyms:23583-46-2;NSC76353;1-(3-o-acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione;23714-40-1;DTXSID10946384;DTXSID90291546;NSC-76353;ZINC04887327;1-[3-O-Acetyl-2-deoxy-5-O-(triphenylmethyl)pentofuranosyl]-4-hydroxy-5-methylpyrimidin-2(1H)-one

Chemical Property of 1-(3-o-Acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione

Chemical Property:

• Density: 1.31g/cm³
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 9
• Exact Mass: 526.21038668
• Heavy Atom Count: 39
• Complexity: 871

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CN(C(=O)NC1=O)C2CC(C(O2)COC(C3=CC=CC=C3)(C4=CC=CC=C4)C5=CC=CC=C5)OC(=O)C

Technology Process of 1-(3-o-Acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione

There total 3 articles about 1-(3-o-Acetyl-2-deoxy-5-o-tritylpentofuranosyl)-5-methylpyrimidine-2,4(1h,3h)-dione 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: 95.0%

acetic anhydride (108-24-7) + 5'-O-tritylthymidine (7791-71-1) → 3'-O-acetyl-5'-O-triphenylmethylthymidine (23583-46-2)

Guidance literature:

With pyridine; at 10 ℃; for 14h;

DOI:10.1016/S0040-4020(97)00141-5

Reference yield:

trityl chloride (76-83-5) → 3'-O-acetyl-5'-O-triphenylmethylthymidine (23583-46-2)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine

2: pyridine

With pyridine;

DOI:10.1039/jr9530000951

Reference yield:

→ 3'-O-acetyl-5'-O-triphenylmethylthymidine (23583-46-2)

Guidance literature:

1b, 1) Triphenylchlormethan, 2) Ac2O;

upstream raw materials:

acetic anhydride

5'-O-tritylthymidine

trityl chloride

Downstream raw materials:

3'-O-acetyl-N³-benzyl-5'-O-trityl thymidine

3-allyloxy-2-formyl-5-(N³-benzyl thymin-1-yl)-tetrahydrofuran

3'-O-allyl-N³-benzyl thymidine

9-benzyl-2-[N³-benzyl-5-methyl-2,4(1H,3H)-pyrimidinedion-1-yl]-perhydro-6,8-(epoxyimino)furo[3,2-b]oxepin