HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805839Generated: October 26, 2026
4-Aminobenzonitrile → HCID 57693596, compound
https://huagongshe.com/reaction/1805839
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile | HCID 57693577 | — |
| Product | HCID 57693596 | HCID 57693596 | 65.4% |
Reaction Steps
To a solution of 4-aminobenzonitrile (54 mg, 0.46 mmol) in 1-methyl-2-pyrridone (1 mL) was added NaH (18 mg, 0.46 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 4-(7-benzyl-2-fluoro-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile (34 mg, 0.091 mmol) in 1-methyl-2-pyrridone (1 mL) was added to the mixture. The mixture was stirred at room temperature for 1 h, poured into ice water, and extracted with EtOAc (2×20 mL). The combined organic solution was washed with H2O (20 mL) and brine (20 mL), dried with Na2SO4, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 28 mg (65%) of 4-[7-benzyl-2-(4-cyano-phenylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy]-3,5-dimethyl-benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354532B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-900f64d671d246d1b8f3f04671db318b |
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| Source note | uspto-grants-2013_01 |
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