C₁₈H₁₇N₇O₂

Base Information

Chemical Name:C₁₈H₁₇N₇O₂
CAS No.:1616484-38-8
Molecular Formula:C₁₈H₁₇N₇O₂
Molecular Weight:363.379
Hs Code.:

C<sub>18</sub>H<sub>17</sub>N<sub>7</sub>O<sub>2</sub>

Synonyms:

Suppliers and Price of C₁₈H₁₇N₇O₂

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 0 raw suppliers

Chemical Property of C₁₈H₁₇N₇O₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₈H₁₇N₇O₂

There total 4 articles about C₁₈H₁₇N₇O₂ 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:

: 1616484-30-0
ethyl (E)-2-(4-(((dimethylamino)methylene)amino)-3-ethynyl-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate

: 1616484-38-8
C₁₈H₁₇N₇O₂

Guidance literature:: Multi-step reaction with 2 steps

1: sodium azide; ; L-proline; sodium L-ascorbate; sodium carbonate / water; dimethyl sulfoxide / 0.5 h / 130 °C / Microwave irradiation

2: ammonia / water; dimethyl sulfoxide / 2 h

With sodium azide; ammonia; sodium carbonate; sodium L-ascorbate; L-proline; In water; dimethyl sulfoxide;
DOI:10.1039/c4ob00904e

Reference yield:

: 1616484-20-8
ethyl 2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)acetate

: 1616484-38-8
C₁₈H₁₇N₇O₂

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 18 h / 60 °C / Sealed tube; Inert atmosphere

2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 18 h / 20 °C / Sealed tube; Inert atmosphere

3: Amberlite? IRA 900 F^-form / chloroform / 18 h / 20 °C / Inert atmosphere

4: sodium azide; ; L-proline; sodium L-ascorbate; sodium carbonate / water; dimethyl sulfoxide / 0.5 h / 130 °C / Microwave irradiation

5: ammonia / water; dimethyl sulfoxide / 2 h

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; ammonia; sodium carbonate; sodium L-ascorbate; triethylamine; L-proline; In chloroform; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 2: |Sonogashira Cross-Coupling;
DOI:10.1039/c4ob00904e

Reference yield:

: 163622-50-2
4-amino-5-iodo-7H-pyrrolo[2,3‐d]pyrimidine

: 1616484-38-8
C₁₈H₁₇N₇O₂

Guidance literature:: Multi-step reaction with 6 steps

1: caesium carbonate / N,N-dimethyl-formamide / 18 h / 0 - 20 °C / Sealed tube; Inert atmosphere

2: N,N-dimethyl-formamide / 18 h / 60 °C / Sealed tube; Inert atmosphere

3: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / N,N-dimethyl-formamide / 18 h / 20 °C / Sealed tube; Inert atmosphere

4: Amberlite? IRA 900 F^-form / chloroform / 18 h / 20 °C / Inert atmosphere

5: sodium azide; ; L-proline; sodium L-ascorbate; sodium carbonate / water; dimethyl sulfoxide / 0.5 h / 130 °C / Microwave irradiation

6: ammonia / water; dimethyl sulfoxide / 2 h

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; ammonia; sodium carbonate; caesium carbonate; sodium L-ascorbate; triethylamine; L-proline; In chloroform; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 3: |Sonogashira Cross-Coupling;
DOI:10.1039/c4ob00904e