HuagongsheHuagongshe Chemistry Print Report · For research reference only
4(5H)-Thiazolone, 2-amino- → 4-[2-Fluoro-4-[(2-imino-4-oxo-1,3-thiazolidin-5-ylidene)methyl]phenoxy]naphthalene-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4(5H)-Thiazolone, 2-amino- | HCID 11175 | — |
| Reactant | 4-(2-Fluoro-4-formyl-phenoxy)-naphthalene-1-carbonitrile | HCID 86623141 | — |
| Product | 4-[2-Fluoro-4-[(2-imino-4-oxo-1,3-thiazolidin-5-ylidene)methyl]phenoxy]naphthalene-1-carbonitrile | HCID 140529023 | — |
Reaction Steps
4-[2-Fluoro-4-(2-imino-4-oxo-thiazolidin-5-ylidenemethyl)-phenoxy]-naphthalene-1-carbonitrile was prepared using 2-amino-thiazol-4-one and 4-(2-Fluoro-4-formyl-phenoxy)-naphthalene-1-carbonitrile following General Procedure C. 1H NMR (400 MHz, DMSO-d6) δ 9.54 (br, 1H), 9.25 (br, 1H), 8.42 (d, J=8.21 Hz, 1H), 8.15 (d, J=8.21 Hz, 1H), 8.08 (d, J=7.82 Hz, 1H), 7.91 (m, 1H), 7.81 (m, 1H), 7.7 (dd, J=12.13 and 2.34 Hz, 1H), 7.64 (s, 1H), 7.49-7.57 (2H), 6.93 (d, J=7.83 Hz, 1H). LC/MS (m/z) [M+1]+390.2 (calculated for C21H13FN3O2S 390.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580832B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-5e7b6bd506cb4c87a1da682dbf2c631d |
| Source note | uspto-grants-2013_11 |