HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 10117133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 10613276 | HCID 10613276 | — |
| Reactant | HCID 12786364 | HCID 12786364 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10117133 | HCID 10117133 | — |
Reaction Steps
Prepared analogously to Example 9 from from 5-(4-methoxybenzenesulfonyl)thiazolidine-2,4-dione and 4′-bromomethyl-4-chlorobiphenyl in N,N-dimethylformamide. Trituration with diethyl ether provided an off-white solid. 1H NMR: δ 7.99 (s, 1H), 7.93 (dm, J=9.0 Hz, 2H), 7.45-7.49 (m, 4H), 7.38-7.41 (m, 2H), 7.23-7.26 (m, 2H), 7.06 (dm, J=9.0 Hz, 2H), 3.97, (A of AB, J=13.7 Hz, 1H), 3.92 (s, 3H), 3.39 (B of AB, J=13.7 Hz, 1H). MS (m/e): 486.0 & 488.0 (M−H)−Cl isotopes. Anal: Calc for C23H18ClNO5S2.C3H7NO: 55.66% C, 4.49% H, 4.99% N; Found: 55.57% C, 4.41% H, 4.85% N. MP: 197-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06716862B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-0ba3fa69ad6a49aa9516cf81cac246c6 |
| Source note | uspto-grants-2004_04 |