Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161854Generated: October 31, 2026

HCID 59519059, compound → HCID 59519057, compound

https://huagongshe.com/reaction/1161854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59519059HCID 59519059—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductHCID 59519057HCID 59519057100%

Reaction Conditions

Temperature70 °C

Reaction Steps

In a capped 20 mL scintillation vial, a mixture of 2-[6-bromo-2-(3-chlorophenyl)-4-oxo-1,4-dihydro-2H-quinazolin-3-yl]-N-tert-butylacetamide (0.51 g, 1.13 mmol) and manganese(IV) dioxide (0.44 g, 5.10 mmol) in chloroform (10 mL) was heated at 70° C. for 3 h. The black suspension was cooled to room temperature, filtered through a pad of celite and concentrated in vacuo to provide 2-[6-bromo-2-(3-chlorophenyl)-4-oxo-4H-quinazolin-3-yl]-N-tert-butylacetamide (INTERMEDIATE VI.1) (0.51 g, 1.13 mmol, 100%) as a white solid. Data for 2-[6-bromo-2-(3-chlorophenyl)-4-oxo-4H-quinazolin-3-yl]-N-tert-butylacetamide (INTERMEDIATE VI.1): 1H NMR (300 MHz, CDCl3): δ 9.44 (d, 1H), 7.86 (dd, 1H), 7.65-7.54 (m, 2H), 7.53-7.4 (m, 3H), 5.47 (s, 1H), 4.46 (s, 2H), 1.34 (s, 9H) ppm; MS (ESI) m/z: 448/450 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820649B2
Source datasetuspto-grants-2010_10
ORD IDord-92019c3da7684f82b87fb6ffbfee6ae9
Source noteuspto-grants-2010_10