HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzenesulfonyl chloride → 5-[4-(4-Fluoro-benzenesulfonyl)-piperazin-1-yl]-quinazoline-2,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 5-Piperazin-1-yl-quinazoline-2,4-diamine | HCID 18071318 | — |
| Product | 5-[4-(4-Fluoro-benzenesulfonyl)-piperazin-1-yl]-quinazoline-2,4-diamine | HCID 25005933 | 41% |
Reaction Steps
Title compound was prepared via Resin Method using 5-piperazin-1-yl-quinazoline-2,4-diamine (50 mg; 0.2 mmol) and 4-fluorobenzene-sulfonyl chloride (79.8 mg; 0.41 mmol) to obtain 33.2 mg. (41% yield). 1H NMR (500 MHz, DMSO-d6) δ 8.35 (s, 1H), 7.89 (m, 2H), 7.54 (t, J=8.5 Hz, 2H), 7.38 (t, J=7.5 Hz, 1H), 6.97 (d, J=8.5 Hz, 1H), 6.93 (s, 1H), 6.83 (d, J=8.0 Hz, 1H), 5.92 (br s, 2H), 3.73 (d, J=11.5 Hz, 2H), 3.11 (d, J=12.0 Hz, 2H), 2.85 (t, J=11.5 Hz, 1H), 2.59 (t, J=11.5 Hz, 2H). ESIMS+404.4.5 m/z
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985755B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-e6a4807743cc442d959d7e4fc083fc2f |
| Source note | uspto-grants-2011_07 |