HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → HCID 10278583, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| Product | HCID 10278583 | HCID 10278583 | — |
Reaction Steps
A solution of 5-bromo-2,4-dichloropyrimidine (228 mg, 1.0 mmol), 4-sulphanilamide (180 mg, 1.05 mmol) and N,N-diisopropylethylamine (174 μl 1.0 mmol) in n-butanol (30 ml) was heated at 100° C. for 16 hours. A gum formed out of solution. Diethyl ether (20 ml) was added, causing the gum to solidify, and further precipitation to occur. The solid was collected by filtration and triturated with hot methanol, giving the title product (55 mg) as a white solid. NMR: (s, 2H), 7.30 (s, 2H), 7.64 (d, 2H), 7.80 (m, 4H), 7.88 (d, 2H), 8.36 (s, 1H), 8.93 (s, 1H), 9.88 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153964B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-db0b9fd7a96041ff8eca65238ff4a01e |
| Source note | uspto-grants-2006_12 |