HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244910Generated: November 1, 2026
1-Butanol → 2-chloro-N-[(3-iodophenyl)-methyl]-9-(tetrahydro-3-thienyl)-9H-purin-6-amine
https://huagongshe.com/reaction/1244910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 3-Iodobenzylamine | HCID 97012 | — |
| Reactant | 2,6-dichloro-9-(tetrahydro-3-thienyl)-9H-purine | HCID 21922991 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-chloro-N-[(3-iodophenyl)-methyl]-9-(tetrahydro-3-thienyl)-9H-purin-6-amine | HCID 21922994 | — |
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 0.114 ml of 3-iodo-benzenemethanamine in place of the benzylamine and the reaction medium is taken to a temperature of approximately 80 to 85° C. for approximately 30 hours, left to return to ambient temperature, diluted with 3 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 90/10, 173 mg of expected product is thus obtained in the form of white-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07122669B1 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-baffa38d22f94dcba6a66410f31593a2 |
|---|
| Source note | uspto-grants-2006_10 |
|---|