HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dabco → 2,4-Diamino-6-(3,4-dichlorophenylsulfinyl)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 6-[(3,4-Dichlorophenyl)sulfanyl]quinazoline-2,4-diamine | HCID 44264142 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,4-Diamino-6-(3,4-dichlorophenylsulfinyl)quinazoline | HCID 12555978 | — |
Reaction Steps
A suspension of 5.0 grams (0.011 mole) of the bromine complex of 1,4-diazabicyclo(2,2,2)octane in 200 mL of aqueous 70% acetic acid was stirred, and 3.4 grams (0.01 mole) of 2,4-diamino-6-(3,4-dichlorophenylthio)quinazoline was added portionwise during about a 1 hour period. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 20 hours. After this time, the reaction mixture was neutralized with concentrated ammonium hydroxide. The resultant solid was collected by filtration and triturated with methanol. The solid was collected by filtration and dried, yielding 2,4-diamino-6-(3,4-dichlorophenylsulfinyl)quinazoline, mp 200° C., dec. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616718 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-ef29a30e667643a58f11b9fcbd0097d0 |
| Source note | uspto-grants-1997_04 |