HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24944550, compound → HCID 131730797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24944550 | HCID 24944550 | — |
| Reactant | HCID 131730798 | HCID 131730798 | — |
| Product | HCID 131730797 | HCID 131730797 | — |
Reaction Steps
This compound was prepared from 5-azetidin-3-yl-1-(benzensulfonyl)-1H-indole by the method outlined for compound 4. ESI-MS [m/z]: 355.15 [M+H]+. 1H-NMR (500 MHz, d6-DMSO): δ=10.8 (bs, 1H), 7.95 (d, 2H), 7.9 (d, 1H), 7.85 (d, 1H), 7.7 (d, 2H), 7.6 (m, 2H), 7.4 (m, 1H), 6.85 (d, 1H), 4.4 (bs, 2H), 4.3 (bs, 1H), 4.1 (bs, 2H), 3.15 (bs, 2H), 1.55 (m, 2H), 0.95 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507469B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-c5326c8d8fdb47ed9ccb50e12cad66a0 |
| Source note | uspto-grants-2013_08 |