HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Aminoethyl)-2,6-dimethoxyphenol → HCID 67242173, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Aminoethyl)-2,6-dimethoxyphenol | HCID 533955 | — |
| Reactant | 4-Chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide | HCID 67243160 | — |
| Product | HCID 67242173 | HCID 67242173 | — |
Reaction Steps
The title compound was prepared from 4-chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide and 4-(2-aminoethyl)-2,6-dimethoxyphenol in a similar manner as described for Example 118. 1H NMR (THF-d8, 500 MHz): δ 1.53 (d, 6H), 2.45 (t, 2H), 3.11 (q, 2H), 3.73 (s, 6H), 4.31-4.39 (m, 1H), 6.03 (s, 2H), 6.47 (t, 1H), 7.22 (s, 1H), 7.46-7.50 (m, 3H), 7.55-7.57 (m, 2H); 13C NMR (125 MHz, THF-d8): δ 19.57, 35.92, 45.47, 46.98, 55.93, 106.13, 106.56, 126.64, 127.87, 128.56, 129.34, 131.86, 135.49, 135.64, 148.12, 158.61; Mass Spectrum: M+H+ 447.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723333B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-65b9a1f2c4e34ba9b94d7167faae8e8e |
| Source note | uspto-grants-2010_05 |