HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431086Generated: November 2, 2026
Dimethyl Sulfoxide → Tert-butyl 6-(6-nitropyridin-3-yl)-2,6-diazaspiro[3.3]heptane-2-carboxylate
https://huagongshe.com/reaction/1431086
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Reactant | 2-Boc-2,6-diazaspiro(3.3)heptane | HCID 40151981 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 6-(6-nitropyridin-3-yl)-2,6-diazaspiro[3.3]heptane-2-carboxylate | HCID 66742261 | — |
Reaction Steps
In a 25 mL pear-shaped flask, tert-butyl 2,6-diazaspiro[3.3]heptane-2-carboxylate (2.81 g, 14.2 mmol), 5-bromo-2-nitropyridine (2.88 g, 14.2 mmol), and TEA (1.58 g, 2.17 ml, 15.6 mmol) were combined with DMSO (12 ml) to give a light yellow solution. The reaction mixture was heated to 90° C. and stirred for 40 h. Cooled to 25° C. and the reaction mixture was diluted with 50 mL H2O and extracted with EtOAc (3×50 mL). The organic layers were combined, washed with sat NaCl (1×50 mL), dried over Na2SO4 and concentrated in vacuo. The purple oil was used crude in the subsequent reduction. (M+H)+=321 m/e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940741B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-206edfe5e8c94f719a8d30756dd071cb |
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| Source note | uspto-grants-2015_01 |
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