HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Azetidinamine, 1-(2-pyridinyl)- → HCID 67242299, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Azetidinamine, 1-(2-pyridinyl)- | HCID 56965702 | — |
| Reactant | 4-Chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide | HCID 67243160 | — |
| Product | HCID 67242299 | HCID 67242299 | — |
Reaction Steps
The title compound was prepared from 4-chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide and 1-pyridine-2-ylazetidin-3-amine in a similar manner as described for Example 118. 1H NMR (500 MHz CDCl3): δ 1.57 (d, 6H), 3.71-3.75 (m, 2H), 3.84 (t, 2H), 4.04-4.10 (m, 1H), 4.37-4.45 (m, 1H), 5.71-5.76 (m, 1H), 6.19 (d, 1H), 6.60-6.64 (m, 1H), 7.40-7.44 (m, 1H), 7.46-7.52 (m, 5H), 8.10-8.12 (m, 1H); 13C NMR (125 MHz CDCl3): δ 20.36, 44.88, 48.00, 58.15, 106.25, 109.08, 113.90, 124.58, 129.24, 130.35, 131.46, 134.60, 137.46, 148.39, 158.35, 160.10; Mass Spectrum: M+H+ 399.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723333B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-b342f35dc82c40f2b446d6681cec9a6a |
| Source note | uspto-grants-2010_05 |