HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-(4-Fluorophenyl)-N-[2-(pyrrolidin-1-yl)ethyl]thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(2-Chloroethyl)pyrrolidine hydrochloride | HCID 81668 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | N-(4-Fluorophenyl)thiazol-2-amine | HCID 25093329 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Fluorophenyl)-N-[2-(pyrrolidin-1-yl)ethyl]thiazol-2-amine | HCID 60204514 | — |
Reaction Steps
A solution of 1.0 g (5.2 mmol) of N-(4-fluorophenyl)thiazol-2-amine in 25 mL of THF was treated with 10.3 mL (10.3 mmol) of a 1.0 M solution of NaHMDS in THF and 0.88 g (5.2 mmol) of 1-(2-chloroethyl)pyrrolidine hydrochloride and heated at reflux for 18 h. The reaction mixture was poured into 250 mL of EtOAc and extracted thrice with 1 M aqueous HCl. The combined acidic extracts were brought to pH 12 with a 10% (w/v) solution of Na2CO3 and extracted five times with CHCl3. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo, and the crude product was purified by flash chromatography eluting with a linear gradient of neat EtOAc to 20% MeOH in EtOAc to deliver the desired compound. MS (M+H)+ 292.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858785B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-2516e22f2d4049c8aa7246ea2491e8aa |
| Source note | uspto-grants-2010_12 |