HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 18328986, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,3,4,9-Tetrahydro-6-methoxy-1-methyl-1H-pyrido(3,4-b)indole | HCID 71028 | — |
| Catalyst | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18328986 | HCID 18328986 | — |
Reaction Steps
To a solution of 700 mg (3.24 mmol) 1-methyl-6-methoxy-1,2,3,4-tetrahydro-β-carboline, and 5 drops NH4OH in ethyl acetate was added 0.4 mL (3.88 mmol) acetic anhydride under N2 gas. The reaction was stirred for 20 min. and then washed with water. The organic layer collected was dried over MgSO4, filtered, and concentrated in vacuo to a dark oil. The oil was dissolved in methanol and chromatographed on reverse phase C-18 using methanol and water. The product was collected and concentrated to a white solid, which showed characteristic peaks: NMR (CDCl3) δ: 1.45 ppm (d, 3H), 2.25 ppm (s, 3H), 3.85 ppm (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314908 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-36e5f3b52127447b84cfc08d4bcd774f |
| Source note | uspto-grants-1994_05 |