HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,1-Trimethoxy-2-chloroethane → 7-Bromo-2-(chloromethyl)quinazolin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,1-Trimethoxy-2-chloroethane | HCID 144702 | — |
| Reactant | 2-Amino-4-bromobenzamide | HCID 13805507 | — |
| Product | 7-Bromo-2-(chloromethyl)quinazolin-4-ol | HCID 135682060 | — |
Reaction Steps
Reflux a solution of 2-amino-4-bromobenzamide (27 g, 0.13 mol; see Joshi and Chaudhari, (1987) Indian J. Chem., Sect. B, 26B(6):602-4) in 2-chloro-1,1,1-trimethoxyethane (50 mL) for 30 minutes, during which time a large precipitate appears. Evaporate the mixture fully and triturate with ether to collect 28 g of 7-bromo-2-chloromethyl-3H-quinazolin-4-one as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074799B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-bb4891bb14ab4be5a0f03b575865206f |
| Source note | uspto-grants-2006_07 |