HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 25074324, compound → HCID 131730799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 25074324 | HCID 25074324 | — |
| Reactant | HCID 131730798 | HCID 131730798 | — |
| Product | HCID 131730799 | HCID 131730799 | — |
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 4. ESI-MS [m/z]: 422.15 [M+H]+. 1H-NMR (500 MHz, d6-DMSO): δ=10.75 (bs, 1H), 8.55 (s, 1H), 8.1 (d, 2H), 7.9 (m, 5H), 7.7 (s, 1H), 7.4 (m, 1H), 6.85 (d, 1H), 4.4 (m, 2H), 4.25 (m, 1H), 4.1 (m, 2H), 3.15 (m, 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-9eb2fe4436a546339fca03a9f835b5c5 |
| Source note | uspto-grants-2013_08 |