HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850302Generated: October 25, 2026
1,2-Dichloroethane → 2,6-Dichloroquinazoline
https://huagongshe.com/reaction/1850302
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Nitric acid, 1,1-dimethylethyl ester | HCID 164756 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Chloroquinazolin-2-amine | HCID 21183942 | — |
| Product | 2,6-Dichloroquinazoline | HCID 12413928 | 20% |
Reaction Steps
To a suspension of 6-chloro-quinazolin-2-ylamine (110) (2.8 g, 15.8 mmol) and SbCl3 (7.2 g, 32 mmol) in 1,2-dichloroethane (100 mL) was added tert-butylnitrate (6.2 ml, 52 mmol) and heated at 60° C. for 3 h under nitrogen atmosphere. To the mixture was added aqueous saturated NaHCO3 and the mixture was filtered off and filtrate was extracted with CHCl3. The organic layer was washed with brine, dried over Na2SO4, and evaporated. The residue was purified by silica gel column chromatography, using CHCl3/EtOAc (9:1, v/v) as eluent to give 2,6-dichloro-quinazoline (111) (0.65 g, 3.12 mmol, 20% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957073B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-114dc365ca4b49cbb0c43ace77126036 |
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| Source note | uspto-grants-2015_02 |
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