HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropylamine → N-cyclopropyl-7-fluoroquinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 4-Chloro-7-fluoroquinazoline | HCID 16227013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclopropyl-7-fluoroquinazolin-4-amine | HCID 25059697 | 80% |
Reaction Steps
4-Chloro-7-fluoro-quinazoline (0.73 g, 4 mmol) and cyclopropylamine (0.23 g, 4 mmol) are stirred in dichloromethane at ambient temperature overnight. The solid product is precipitated with hexanes, filtered, and washed with hexane and ethyl acetate, affording 0.3 g of desired Cyclopropyl-(7-fluoro-quinazolin-4-yl)-amine. The filtrate is concentrated and precipitated with hexanes, yielding an additional 0.35, for a combined yield of 80%. LC/MS m/z=204 [M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-d3116dd597eb4c88bb4beaff3f2791ad |
| Source note | uspto-grants-2010_03 |