HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinamide → HCID 68825648, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinamide | HCID 21864724 | — |
| Reactant | HCID 68827324 | HCID 68827324 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68825648 | HCID 68825648 | 72% |
Reaction Steps
N-Iodosuccinamide (0.030 g, 0.13 mmol, 1.0 eq) was added to a solution of ethyl 1H-pyrrolo[3,2-c]pyridin4-ylcarbamate (0.027 g, 0.13 mmol, 1.0 eq) in THF (1 mL) at room temperature and the reaction mixture was stirred for 15 minutes. The reaction mixture was quenched with 10% NaHSO3 solution and extracted with 10/1 CHCl3/MeOH. The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, eluting 0-5% CHCl3/MeOH) to afford the product (0.031 g, 72%) as a solid. 1H NMR (CD3OD) δ 7.87 (d, 1H, J=5.9 Hz), 7.38 (s, 1H), 7.25 ((d, 1H, J=5.9 Hz), 4.14 (q, 2H, J=7.1 Hz), 1.12 (t, 3H, J=7.1 Hz); MS(ESI+) m/z 332 (M+H)+. Calculated: 331.9896, found: 331.9884.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566784B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-860dc91cc27a4ada811af96293f21ffb |
| Source note | uspto-grants-2009_07 |