HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzenepropanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine | HCID 219752 | — |
| Reactant | phenylalaninol, (R)- | HCID 853475 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzenepropanol | HCID 31234 | 74% |
Reaction Steps
First, 1.13 g of the starting material 4-chloro-1-phenylpyrazolo[3,4-d]pyrimidine was combined with 0.67 ml Et3N, 0.74 g of (R)-(+)-2-amino-3-phenyl-1-propanol in 60 ml absolute ethanol and heated in a steam bath for four hours. The solvent was then removed under vacuum and the residue was purified by flash chromatography (10-20% isopropyl alcohol/hexane) to yield 1.24 g of (R)-β-[1-phenyl-1H-pyrazolo-[3,4-d]pyrimidin-4-yl)amino]benzenepropanol (74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05086176 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-911669d008d041b38b40a5cc2bc10729 |
| Source note | uspto-grants-1992_02 |