HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 46899292, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11453978 | HCID 11453978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46899292 | HCID 46899292 | 48.5% |
Reaction Steps
To a stirred solution of 57 mg (0.123 mmol) of (RS,SR)-C-{5-[benzenesulfonyl-(7-chloro-1,2,3,4-tetrahydro-cyclopenta[b]indol-2-yl)-fluoro-methyl]-[1,2,4]oxadiazol-3-yl}-methylamine in 5 mL of THF, 20 μL (0.123 mmol, 1 eq) of Huenig base and 11.6 μL (0.123 mmol, 1 eq) of acetic anhydride were added at 0° C. After 30 min., the reaction mixture was quenched by addition of an aqueous solution of NaHCO3 and extracted with CH2Cl2. The combined organic phases were dried over Na2SO4, filtered and evaporated. Column chromatography on silica gel gave 30 mg (48%) of (RS,SR)-N-{5-[benzenesulfonyl-(7-chloro-1,2,3,4-tetrahydro-cyclopenta[b]indol-2-yl)-fluoro-methyl]-[1,2,4]oxadiazol-3-ylmethyl}-acetamide as a light yellow solid, MS: 503 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906546B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-bbaf13a5bb7241cb97e8237894439ea4 |
| Source note | uspto-grants-2011_03 |