HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Isopropoxy-phenyl)-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Isopropoxyaniline | HCID 82112 | — |
| Reactant | 2-Chloro-7H-pyrrolo[2,3-d]pyrimidine | HCID 5706774 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (4-Isopropoxy-phenyl)-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-amine | HCID 68639256 | — |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
To a suspension of 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (700 mg, 4.33 mmol) in BuOH (10 mL) is added 4-isopropoxyaniline (1.31 g, 8.66 mmol) and concentrated aqueous HCl (37%, 1.28 mL, 13.0 mmol). The reaction mixture is heated to 140° C. for 24 h, cooled to rt, and concentrated under reduce pressure. The residue is dissolved in EtOAc and the organic layer is washed with saturated aqueous Na2CO3 solution (2×). The organic layer is dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue solid residue is triturated with hexane to yield the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420657B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-7b1b1fe4ef4f428883eb08f2c2b1aec8 |
| Source note | uspto-grants-2013_04 |