Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 86687568 | HCID 86687568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 86687570 | HCID 86687570 | — |
Reaction Steps
A flask containing a solution of 2-aminothiazole (0.039 g, 0.386 mmol) and perfluorophenyl 4-chloro-6-fluoroquinoline-7-sulfonate (0.150 g, 0.351 mmol) in THF (1.754 ml) was cooled to −78° C. for 10 minutes, and then lithium bis(trimethylsilyl)amide, 1.0 m solution in tetrahydrofuran (0.701 ml, 0.701 mmol) was added drop wise (conversion from colorless solution to yellow-orange). After 20 minutes, the reaction was diluted with sat. aq ammonium chloride solution, and was extracted with DCM:MeOH (90:10) (×3). The organics were dried over sodium sulfate, filtered and concentrated in vacuo. The material was taken forward crude. m/z (ESI) 344.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012443B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-960a33a11c604ee5b18a25d0fb5b3102 |
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| Source note | uspto-grants-2015_04 |
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