HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-methylbutane → 2-[(5-chloro-1H-indol-3-yl)methyl]-5-methyl-7-(3-methylbutyl)-3-(1-methyl-1H-imidazol-2-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-[(5-chloro-1H-indol-3-yl)methyl]-5-methyl-3-(1-methyl-1H-imidazol-2-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione | HCID 136334114 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(5-chloro-1H-indol-3-yl)methyl]-5-methyl-7-(3-methylbutyl)-3-(1-methyl-1H-imidazol-2-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione | HCID 58981092 | — |
Reaction Steps
This compound was synthesized by the reaction of 2-[(5-chloro-1H-indol-3-yl)methyl]-5-methyl-3-(1-methyl-1H-imidazol-2-yl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione and 1-bromo-3-methylbutane using potassium carbonate as a base in DMF at 80° C. Mass: 480.16 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07285558B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-c38e935d2ebc4e0bbcf9cda77a833414 |
| Source note | uspto-grants-2007_10 |