HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709819Generated: October 31, 2026
Hydrochloric Acid → HCID 117759910, compound
https://huagongshe.com/reaction/709819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 117759967 | HCID 117759967 | — |
| Reactant | Ethyl 3-(6-chloropyrimidin-4-yl)-3-cyclopropylpropanoate | HCID 117760030 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117759910 | HCID 117759910 | 58.6% |
Reaction Steps
Under a nitrogen atmosphere, to a solution of (5-(2-fluoro-5-methoxyphenyl)-4-isobutoxypyrimidin-2-yl)methanol (111 mg) and ethyl 3-(6-chloropyrimidin-4-yl)-3-cyclopropylpropanoate (92 mg) in THF (2.0 mL) was added 60% sodium hydride (17 mg) at room temperature, and the mixture was stirred at 50° C. for 2 hr. To the reaction mixture was added 1N hydrochloric acid at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (111 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181186B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-f97e7ed824274c0bbb12f88f3ccd5c9e |
|---|
| Source note | uspto-grants-2015_11 |
|---|