HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013776Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 59427365, compound
https://huagongshe.com/reaction/1013776
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (5-(4-(4-(7-Methoxy-1,5-naphthyridin-4-yloxy)phenylamino)phthalazin-1-yl)thiophen-3-yl)methanol | HCID 59427351 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59427365 | HCID 59427365 | — |
Reaction Steps
A round bottom flask was charged with (5-(4-(4-(7-methoxy-1,5-naphthyridin-4-yloxy)phenylamino)phthalazin-1-yl)thiophen-3-yl)methanol (71 mg, 140 μmol) and 2.8 mL DCM, and the mixture was cooled to 0° C. under nitrogen. (Diethylamino) trifluorosulfur (55 μl, 420 μmol) was added, and the mixture was stirred at 0° C. for 20 min and was then allowed to warm to RT. After another 0.5 h, saturated NaHCO3 was added and the mixture was stirred for 10 min. The solids were filtered, and the crude material was purified by silica gel chromatography, 90/10/1 DCM/MeOH/NH4OH in DCM, followed by reverse phase chromatography, Gilson, 10-90% 0.1% TFA/ACN in water, to provide the titled compound. MS: [M+H]=510.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981891B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-5463051436d841e690de4b23fca34981 |
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| Source note | uspto-grants-2011_07 |
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