HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57843Generated: October 26, 2026
Diisopropylethylamine → tert-Butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate
https://huagongshe.com/reaction/57843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-6-fluoropyridine | HCID 639438 | — |
| Reactant | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate | HCID 70700340 | 50.1% |
Reaction Steps
A mixture of 2-bromo-6-fluoropyridine (500 mg, 2.8 mmol), tert-butyl 1,4-diazepane-1-carboxylate (568 mg, 2.8 mmol) in DIPEA (1.83 g, 14.2 mmol) in ethanol (10 mL) was heated at 100° C. for 16 hours. The reaction mixture was concentrated under reduced pressure and the residue was diluted with EtOAc (100 mL). The solution was washed with brine, dried over Na2SO4, and concentrated under reduced pressure to afford tert-butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate as a colorless oil (500 mg, 50%). MS (ESI) m/z: 356 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434725B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-3c81de5258514889bd3738db16a79614 |
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| Source note | uspto-grants-2016_09 |
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