HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Tert-butyl 2,2,2-trichloroethanimidate | HCID 2734700 | — |
| Reactant | 4-methoxy-3-((7-methyl-1H-indazol-5-yl)methyl)-4-oxobutanoic acid | HCID 18452115 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinate | HCID 57794720 | — |
Reaction Steps
To a solution of 4-methoxy-3-((7-methyl-1H-indazol-5-yl)methyl)-4-oxobutanoic acid (0.9764 g, 3.54 mmol) and t-butyl-2,2,2-trichloroacetoimidate (3.78 mL, 21.22 mmol) in tetrahydrofuran (25 mL) was added 1M boron trifluoride etherate (0.2 mL) at room temperature. Heat generation was observed and the reaction was stirred for 3.5 h before passing it through a pad of silica gel. Evaporation of the filtrate gave a white solid. Methylene chloride (20 mL) was added and the resulting white solid was removed by filtration. The filtrate was concentrated and the final product was obtained via silica gel chromatography eluting with 0% to 50% ethyl acetate/hexane. (0.605 g, 52%) HPLC tR=1.51 min, MS(ESI)[M+H]+=332.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569578B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-aa6066628f6c40c8b75a75fca9f74d27 |
| Source note | uspto-grants-2009_08 |