HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide → 1-(Cyclohexylmethyl)indoline-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide | HCID 32103726 | — |
| Reactant | 1-(Cyclohexanecarbonyl)indoline-5-sulfonamide | HCID 60698742 | — |
| Product | 1-(Cyclohexylmethyl)indoline-5-sulfonamide | HCID 34914005 | 57% |
Reaction Steps
Following a procedure analogous to that for the synthesis of Intermediate 53, 1-(cyclohexanecarbonyl)indoline-5-sulfonamide (Intermediate 55, 120 mg, 0.39 mmol) was converted to the title compound (65 mg, 57%) after purification using preparative HPLC. 1H NMR (CD3OD) δ 7.54 (dd, J=8.4, 2.0 Hz, 1H), 7.45 (d, J=1.5 Hz, 1H), 6.38 (d, J=8.4 Hz, 2H), 3.54 (d, J=8.7 Hz, 2H), 3.04-2.96 (m, 4H), 1.80-1.68 (m, 6H), 1.31-1.23 (m, 3H), 1.05-0.96 (m, 2H); MS(ESI+) m/z 295.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346795B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-30ed4f1a09c14cc186f1d1e457b53471 |
| Source note | uspto-grants-2016_05 |