HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645661Generated: October 31, 2026
2-Chloronicotinonitrile → HCID 58996706, compound
https://huagongshe.com/reaction/645661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58996706 | HCID 58996706 | — |
Reaction Steps
2-Chloro-nicotinonitrile (1.0 g, 7.215 mmol) was added to a mixture of [1,4]Diazepane-1-carboxylic acid tert-butyl ester and potassium hydrogencarbonate (0.87 g, 8.66 mmol) in N,N-dimethylformamide (20 mL). The mixture was heated at 90° C. overnight. The reaction mixture was poured onto ice and extracted with dichloromethane. The organic layer was washed with water and brine then dried over magnesium sulfate and filtered. The solvent was removed and the residue was purified by flash column chromatography on silica using ethyl acetate/heptane (50:50) mixture as the mobile phase to give 4-(2-Cyano-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester. 1H-NMR (400 MHz, DMSO-d6) δ 1.25 (d, 27 Hz, 9H), 1.81 (m, 1H), 1.87 (m, 1H), 3.31 (m, 2H), 3.55 (m, 1H), 3.60 (m, 1H), 3.84 (m, 2H), 3.94 (m, 2H), 6.75 (m, 2H), 8.34 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07704997B1 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-fc561597d41c4c77aed294a2ea2d504f |
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| Source note | uspto-grants-2010_04 |
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