HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 1,2,2-trimethyl-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 6-Chloro-9H-beta-carbolin-8-amine | HCID 21362701 | — |
| Reactant | 1,2,2-Trimethyl-5-oxopyrrolidine-3-carboxylic acid | HCID 56737763 | — |
| Product | 1,2,2-trimethyl-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide | HCID 11451546 | 68% |
Reaction Steps
The desired compound was prepared according to Method B from 6-chloro-9H-β-carboline-8-ylamine and 1,2,2-trimethyl-5-oxo-pyrrolidine-3-carboxylic acid in 68% yield. 1H-NMR (DMSO-d6, 300 MHz) δ 1.23 (s, 3H), 1.45 (s, 3H), 2.59 (dd, 1H), 2.66(s, 3H), 2.70 (dd, 1H), 3.17 (t, 1H), 7.91 (m, 1H), 8.18 (d, 1H), 8.24 (d, 1H), 8.40 (d, 1H), 9.07 (s, 1H), 10.16 (s, 1H), 11.32 (s, 1H). Retention Time (LC, method: ammonium acetate standard): 1.17 min. MS (M+H+): 371.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951801B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-8971a0828f544af780491cb5656fc91c |
| Source note | uspto-grants-2011_05 |