HuagongsheHuagongshe Chemistry Print Report · For research reference only
phenylalaninol, (S)- → (S)-beta-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | phenylalaninol, (S)- | HCID 447213 | — |
| Reactant | 4,6-dichloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine | HCID 4737109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-beta-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanol | HCID 15667125 | 97% |
Reaction Steps
2.5 g of the starting material 1-phenyl-4,6-dichloropyrazolo[3,4-d]pyrimidine was suspended in 60 ml of ethanol. Next, 4.28 g of (S)-(-)-2-amino-3-phenyl-1-propanol was added and the reaction was allowed to stir for 24 hours. The solvent was then removed under vacuum and the crude oil was purified by flash chromatography (10-15-20% isopropyl alcohol/hexane) to yield 3.5 g of (S)-β-[(1-phenyl-6-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]benzenepropanol (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064947 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-86082389e41941b6925f0e2b852e457e |
| Source note | uspto-grants-1991_11 |