HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066157Generated: November 2, 2026
Azetidine → (2S)-1-{[6-(1-Azetidinyl)-4-methyl-3-pyridinyl]carbonyl}-2-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine
https://huagongshe.com/reaction/2066157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azetidine | HCID 10422 | — |
| Reactant | (2S)-1-[(6-Fluoro-4-methyl-3-pyridinyl)carbonyl]-2-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine | HCID 59161361 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (2S)-1-{[6-(1-Azetidinyl)-4-methyl-3-pyridinyl]carbonyl}-2-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine | HCID 59161401 | 92.6% |
Reaction Steps
(2S)-1-[(6-Fluoro-4-methyl-3-pyridinyl)carbonyl]-2-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (may be prepared as described in Example 27) (67 mg, 0.15 mmol) was weighed into a microwave vial and dissolved in isopropanol (1.5 ml). Azetidine (0.203 ml, 3.01 mmol) was added and the mixture was heated in the microwave to 120° C. for 12 h with stirring. The reaction mixture was concentrated to give the crude material as a colourless gum (˜187 mg). This was purified by MDAP to give the title compound as a pale yellow gum (67 mg). The gum was redissolved in MeOH, water was added, and the mixture was concentrated under a flow of argon then dried in vacuo to give the title compound as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288388B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5046501f4762415dbccdf6e970a5794d |
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| Source note | uspto-grants-2012_10 |
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