HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640424Generated: October 31, 2026
Hydrochloric Acid → 1-(5-Bromopyridin-2-yl)-1,4-diazepane
https://huagongshe.com/reaction/1640424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1-Dimethylethyl 4-(5-bromo-2-pyridinyl)-1,4-diazepane-1-carboxylate | HCID 60209566 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(5-Bromopyridin-2-yl)-1,4-diazepane | HCID 16784733 | 117.1% |
Reaction Steps
6 ml of a solution of hydrogen chloride (6N) in isopropanol are added to a solution of 1.63 g (4.4 mmol) of 1,1-dimethylethyl 4-(5-bromo-2-pyridyl)-1,4-diazepane-1-carboxylate, obtained in step 11.1, in 12 ml of dioxane and 4 ml of ethanol. This reaction mixture is maintained at 70° C. for 3 hours. The mixture is allowed to cool to room temperature and is then concentrated under reduced pressure. 1.32 g of a white solid are obtained after crystallization from acetone. These crystals are taken up in 10 ml of dichloromethane and the reaction medium is basified to pH=14, by adding 28% ammonia solution. The organic phase is recovered by filtration through a hydrophobic cartridge and the filtrate is concentrated under reduced pressure. 0.96 g of product is obtained in the form of an oil, and is used without further purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114866B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-5c6a86dd77024bb7abecc505e8c77aaa |
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| Source note | uspto-grants-2012_02 |
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