HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251499Generated: October 31, 2026
HCID 53908910, compound → HCID 67268602, compound
https://huagongshe.com/reaction/251499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 53908910 | HCID 53908910 | — |
| Reactant | HCID 178478979 | HCID 178478979 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | HCID 67268602 | HCID 67268602 | — |
Reaction Steps
Phenylmagnesium chloride (1.5 ml of a 2M solution in THF) was added dropwise with stirring under nitrogen to a solution of 4-(4-amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)benzaldehyde (0.25 g) in toluene/THF (1:1, 16 ml) at minus 78° C. under nitrogen. After the addition the mixture was allowed to warm 0° C. and maintained at this temperature for 40 minutes. The reaction was quenched by the dropwise addition of saturated ammonial chloride solution (4 ml) at 0° C. The mixture was allowed to warm to ambient temperature and stood overnight at this temperature. The solvent was removed under reduced pressure and the solid residue obtained was washed with water and filtered. The residue was triturated with hot ethyl acetate, collected by filtration and identified by LCMS as ∝-[4-(4-amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzyl alcohol, m.p. 279-281° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863444B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ad7411334f0e4afca76d2e728954badf |
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| Source note | uspto-grants-2011_01 |
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