HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361422Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 11655097, compound
https://huagongshe.com/reaction/1361422
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 11495851 | HCID 11495851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11655097 | HCID 11655097 | — |
Reaction Steps
A solution of N-[(E)-5-hydroxy-2-adamantyl]-2-{4-[5-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}acetamide (66 mg, 0.15 mmoles) from Example 2 in DCM (0.5 mL) was cooled to −78° C., treated with (diethylamino)sulfur trifluoride (DAST)(0.020 mL, 0.16 mmoles) and slowly warmed to room temperature over 6 hours. The mixture was quenched with aqueous saturated sodium bicarbonate (0.1 mL), filtered through a Celite cartridge and purified (silica gel, 10-15% acetone in hexane) to provide the title compound as a white solid. 1H NMR (300 MHz, CDCl3) δ 8.42 (s, 1H), 7.63 (m, 2H), 6.68 (d, J=9.2 Hz, 1H), 4.09 (d, J=8.5 Hz, 1H), 3.69 (s, 4H), 3.09 (s, 2H), 2.69 (s, 4H), 2.27-2.22 (m, 3H), 2.06 (m, 2H), 1.94 (m, 4H), 1.58-1.54 (m, 4H); (APCI+) m/z 441 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880001B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-84aabddf628a4b5896c6503d388da971 |
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| Source note | uspto-grants-2011_02 |
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