HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391328Generated: October 29, 2026
P,P-Diphenylphosphinic azide → 4-(5-(1-Aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrile
https://huagongshe.com/reaction/391328
Participants
| Role | Name | HCID | Charge |
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| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-(5-(3-Chloro-4-cyanophenyl)pyridin-3-yl)cyclopropanecarboxylic acid | HCID 59578410 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-(1-Aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrile | HCID 59578418 | — |
Reaction Steps
To a solution of 1-(5-(3-chloro-4-cyanophenyl)pyridin-3-yl)cyclopropanecarboxylic acid (900 mg, 3.01 mmol) in toluene (50 mL) was added TEA (0.63 mL, 4.52 mmol) and diphenylphosphoryl azide (0.977 mL, 4.52 mmol), and the mixture was heated to 100° C. for 4 h. The mixture was then cooled to room temperature and concentrated in vacuo. The residue was re-dissolved in THF (100 mL) and a solution of KOtBu (2.03 g, 18.08 mmol) in THF (40 mL) was added. The mixture was stirred at 0° C. for 1 h. The mixture was then warmed to room temperature overnight. Silica gel (10 g) was added and the mixture was concentrated in vacuo. The residue was purified by silica chromatography eluting with a 0-10% MeOH-DCM gradient to give 4-(5-(1-aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrile. m/z 270.0, 272.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383827B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-a69c51cb2fee4dffa9c7aac9d27013a5 |
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| Source note | uspto-grants-2013_02 |
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