HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969512Generated: November 1, 2026
Diisopropylethylamine → HCID 58557985, compound
https://huagongshe.com/reaction/1969512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | 3-(Imidazole-1-sulfonyl)-1-methyl-3H-imidazol-1-ium triflate | HCID 11728149 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58557985 | HCID 58557985 | 55.1% |
Reaction Steps
A solution of 3,3-difluoroazetidine hydrochloride (1.00 g, 7.72 mmol) and DIEA (1.5 mL, 8.6 mmol) in MeCN (5 mL) was stirred for about 5 min and then was added to a solution of 1-(1H-imidazol-1-ylsulfonyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (4.20 g, 11.6 mmol) in MeCN (10 mL) at about 0° C. The reaction mixture was stirred at about 0° C. for about 1 h, and then warmed to ambient temperature and stirred for about 16 h. The reaction mixture was then concd under reduced pressure. The crude material was purified by flash chromatography on silica gel eluting with a gradient of 5-100% EtOAc in DCM to give 1-(3,3-difluoroazetidin-1-ylsulfonyl)-1H-imidazole (0.95 g, 55%) as a yellow solid: LC/MS (Table 1, Method c) Rt=1.16 min; MS m/z 224 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426411B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-277da7afc80d4eaeabdcfba1e669ddc3 |
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| Source note | uspto-grants-2013_04 |
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