HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 25074324, compound → HCID 25069606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 25074324 | HCID 25074324 | — |
| Reactant | HCID 131730800 | HCID 131730800 | — |
| Product | HCID 25069606 | HCID 25069606 | — |
Reaction Steps
This compound was prepared from 5-azetidin-3-yl-1-(4-oxazol-5-yl-benzensulfonyl)-1H-indole by the method outlined for compound 7. ESI-MS [m/z]: 382.05 [M+H]+. 1H-NMR (400 MHz, d6-DMSO): δ=8.7 (bs, 1H), 8.55 (s, 1H), 7.9 (m, 5H), 7.45 (d, 1H), 7.25 (s, 1H), 7.2 (d, 1H), 4.2 (m, 2H), 4.1-3.9 (m, 5H), 2.95 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507469B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-2f5ffc6e98574f549d683204c6d95fb4 |
| Source note | uspto-grants-2013_08 |