HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161854Generated: October 31, 2026
HCID 59519059, compound → HCID 59519057, compound
https://huagongshe.com/reaction/1161854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59519059 | HCID 59519059 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 59519057 | HCID 59519057 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820649B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-92019c3da7684f82b87fb6ffbfee6ae9 |
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| Source note | uspto-grants-2010_10 |
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