HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide → 1-(2-(Phenylthio)ethyl)indoline-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide | HCID 32103726 | — |
| Reactant | 1-(2-(Phenylthio)acetyl)indoline-5-sulfonamide | HCID 71060712 | — |
| Product | 1-(2-(Phenylthio)ethyl)indoline-5-sulfonamide | HCID 71062985 | 57% |
Reaction Steps
Following a procedure analogous to that for the synthesis of Intermediate 53, 1-(2-(phenylthio)acetyl)indoline-5-sulfonamide (Intermediate 66, 74 mg, 0.21 mmol) was converted to the title compound (40 mg, 52%) after purification using preparative HPLC. 1H NMR (DMSO-d6) δ 7.43-7.33 (m, 6H), 7.21 (t, J=7.2. Hz, 1H), 6.90 (s, 2H), 6.36 (d, J=8.4 Hz, 1H), 3.53 (t, J=8.6 Hz, 2H), 3.39 (t, J=6.8 Hz, 2H), 3.19 (t, J=6.9 Hz, 2H), 2.94 (t, J=8.6 Hz, 2H); MS(ESI+) m/z 335.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346795B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-9cb86ddd57574206b32e148a9581c2e2 |
| Source note | uspto-grants-2016_05 |