HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-{[(1S,2S)-2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[(1S,2S)-2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methanamine dihydrochloride | HCID 66720584 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{[(1S,2S)-2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methyl}acetamide | HCID 59334474 | 99% |
Reaction Steps
To a solution of 1-[(1S,2S)-2-(2-methyl-2H-indazol-4-yl)cyclopropyl]methanamine dihydrochloride (300 mg, 1.09 mmol) and triethylamine (305 μL, 2.19 mmol) in tetrahydrofuran (10 mL) was added acetic anhydride (124 μL, 1.31 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (methanol/ethyl acetate=5/95→20/80) to give the title compound (242 mg, yield 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08110585B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-87b5f620265246f1aaa4085193749bf2 |
| Source note | uspto-grants-2012_02 |