HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 2-chloro-N-phenyl-9-(tetrahydro-3-thienyl)-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purine | HCID 21922991 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-chloro-N-phenyl-9-(tetrahydro-3-thienyl)-9H-purin-6-amine | HCID 21922928 | — |
Reaction Steps
The operation is carried out as in Stage 2 of Example 5 starting from 160 mg of the product obtained in Stage 1 of Example 5, 3 ml of butanol and using 0.055 ml of aniline in place of the benzylamine and the reaction medium is taken to a temperature of approximately 80 to 85° C. for 20 hours, left to return to ambient temperature, diluted with 5 ml of isopropanol, placed for approximately one hour at a temperature of approximately 0° C., followed by separating, washing with 5 ml of isopropanol and drying under vacuum to a temperature of approximately 50° C. After purification on silica eluting with methylene chloride/ethyl acetate in a proportion of 90/10, 173 mg of expected product is thus obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122669B1 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-c4132c48fb714a1b9599f843a380f14d |
| Source note | uspto-grants-2006_10 |