HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777922Generated: October 30, 2026
(S)-(+)-3-Hydroxytetrahydrofuran → HCID 95731090, compound
https://huagongshe.com/reaction/1777922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-(+)-3-Hydroxytetrahydrofuran | HCID 2733227 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 2-Amino-4-fluoropyridine | HCID 18327808 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 95731090 | HCID 95731090 | — |
Reaction Steps
(S)-tetrahydrofuran-3-ol (707 mg, 8.03 mmol) was treated with KHMDS (1 M in THF, 5.89 ml, 5.89 mmol) and stirred at room temperature for 5 min. Then, the mixture was added to a solution of 4-fluoropyridin-2-amine (300 mg, 2.68 mmol) in THF (15 ml). The resulting brown solution was stirred for 16 h. KHMDS (1 M in THF, 2.68 ml, 2.68 mmol) was added to the reaction and the reaction mixture was stirred at 50° C. for 16 h. The reaction mixture was quenched with sat. aq. NH4Cl and extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4, filtered and concentrated. The crude material was purified by normal phase chromatography (12 g silica gel cartridge, heptanes/EtOAc 100:0 to 0:100) to give the title compound as a pink solid. (UPLC-MS 3) tR 0.30 min; ESI-MS 181.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09266883B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-49324ea2c95f4fed827d0e57eb936f97 |
|---|
| Source note | uspto-grants-2016_02 |
|---|