7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile

Base Information

Chemical Name:7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile
CAS No.:57071-71-3
Molecular Formula:C13H14N4O5
Molecular Weight:306.2741
Hs Code.:
NSC Number:163648
DSSTox Substance ID:DTXSID60303943

Synonyms:NSC163648;57071-71-3;DTXSID60303943;NSC-163648;7H-Pyrrolo[2, 4-methoxy-7-.beta.-D-ribofuranosyl-

Suppliers and Price of 7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile

Chemical Property:

Vapor Pressure:2.92E-18mmHg at 25°C
Boiling Point:658.9°Cat760mmHg
Flash Point:352.3°C
Density:1.72g/cm³
XLogP3:-1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:306.09641956
Heavy Atom Count:22
Complexity:457

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=NC=NC2=C1C(=CN2C3C(C(C(O3)CO)O)O)C#N

Technology Process of 7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile

There total 6 articles about 7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-methoxypyrrolo[2,3-d]pyrimidine-5-carbonitrile 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: 52.0%

: 124-41-4
sodium methylate

: 52443-16-0
4-chloro-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile

: 57071-71-3
4-methoxy-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile

Guidance literature:: In methanol; for 16h; Heating;
DOI:10.1016/j.bioorg.2006.07.003

Reference yield:

: 57071-68-8
3,4-dihydro-4-oxo-7-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile

: 57071-71-3
4-methoxy-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / phosphorous oxychloride / 1 h / Heating

2: 81.5 percent / ammonia; methanol / 2.5 h / 5 °C

3: 52 percent / methanol / 16 h / Heating

With methanol; ammonia; trichlorophosphate; In methanol;
DOI:10.1016/j.bioorg.2006.07.003

Reference yield:

: 57071-52-0
4-chloro-5-cyano-7-(2',3',5'-tri-O-acetyl-β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine

: 57071-71-3
4-methoxy-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 81.5 percent / ammonia; methanol / 2.5 h / 5 °C

2: 52 percent / methanol / 16 h / Heating

With methanol; ammonia; In methanol;
DOI:10.1016/j.bioorg.2006.07.003