HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576584Generated: October 31, 2026
Benzyl Bromide → 3-benzyl-6-bromoquinazolin-4(3H)-one
https://huagongshe.com/reaction/576584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-bromoquinazolin-4-ol | HCID 135444905 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-benzyl-6-bromoquinazolin-4(3H)-one | HCID 1187507 | 57.2% |
Reaction Steps
Benzyl bromide (0.264 mL, 2.22 mmol) was added to a solution of 6-bromoquinazolin-4(3H)-one (0.5 g, 2.22 mmol) and NaH (0.08 g, 3.33 mmol) in DMF (5 mL) at 0° C. The reaction mixture was heated to 80° C. for 4 h. The reaction mixture was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo to afford title compound (0.4 g, 48.1%) as pale yellow solid. 1H NMR (400 MHz, CDCl3): δ 8.46 (d, J=1.6 Hz, 1H), 8.09 (s, 1H), 7.83 (dd, J1=2.0 Hz, J2=8.8 Hz, 1H), 7.57 (d, J=8.4 Hz, 1H), 7.4-7.2 (m, 5H), 5.2 (s, 2H); ESI-MS m/z=315 (M+H)+; LCMS purity: 84.2%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040517B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-24e00efc82e24fb5a65e4025d99c2b86 |
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| Source note | uspto-grants-2015_05 |
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