HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzenesulfonyl chloride → 1-[(4-Methoxyphenyl)sulfonyl]-4-(1-piperazinyl)-1H-indole Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate | HCID 22015386 | — |
| Product | 1-[(4-Methoxyphenyl)sulfonyl]-4-(1-piperazinyl)-1H-indole Hydrochloride | HCID 10294853 | — |
Reaction Steps
The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 4-methoxyphenylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.07 (br, 1H), 7.90 (d, J=8 Hz, 2H), 7.78 (d, J=5 Hz, 1H), 7.61 (d, J=8 Hz, 1H), 7.25 (t, J=8 Hz, 1H), 7.09 (d, J=8 Hz, 2H), 6.92 (d, J=8 Hz, 1H), 6.68 (d, J=8 Hz, 1H), 3.79 (s, 3H), 3.24 (m, 8H); MS (ESI+) for m/z 371 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524839B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-c22b75d06177457f9f7987b6f0ac31a5 |
| Source note | uspto-grants-2009_04 |