HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-methanesulfonylpyridine → HCID 71487974, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-methanesulfonylpyridine | HCID 13433424 | — |
| Reactant | HCID 68653876 | HCID 68653876 | — |
| Reactant | HCID 71201914 | HCID 71201914 | — |
| Reactant | HCID 84668872 | HCID 84668872 | — |
| Product | HCID 71487974 | HCID 71487974 | — |
Reaction Steps
Prepared analogously to Compound 1 using IM46 and (S)-1-(6-Methanesulfonyl-pyridin-3-yl)-ethylamine (prepared from 1-(6-Methanesulfonyl-pyridine-3-yl)-ethanone analogously to IM24, which was prepared from commercially available 5-Bromo-2-methanesulfonyl-pyridine CAS 98626-95-0). Yield from IM46=1.54 g (68%). 1H-NMR (500 MHz, DMSO) δ 8.80 (d, 1H), 8.72 (s, 1H), 8.02 (m, 2H), 7.27 (m, 2H), 7.20 (s, 1H), 7.12 (d, 2H), 5.08 (m, 1H), 3.27 (s, 3H), 2.20 (m, 1H), 1.95 (m, 1H), 1.42 (d, 3H), 1.37 (m, 1H), 1.22 (m, 1H). LC-MS (m/z) 345.1 (MH+), tR=1.21 min (method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598213B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-40853531d38c4ea383218bd8db2004e2 |
| Source note | uspto-grants-2013_12 |