HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 15947351, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(BOC-amino)-1-pentyl bromide | HCID 4455360 | — |
| Reactant | HCID 67194973 | HCID 67194973 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 15947351 | HCID 15947351 | 58.6% |
Reaction Steps
A mixture of 100 mg of 2-amino-6-chloro-4-(3-hydroxyphenyl)quinazoline hydrochloride, 90.69 mg of 5-(BOC-amino)-1-pentyl bromide, 100 mg of potassium carbonate and 1 ml of DMF is stirred at 40° for 16 hours. The mixture is dissolved in 2 ml of dichloromethane, 1 ml of TFA is added, and the mixture is stirred at room temperature for 4 hours. 3 ml of n-heptane are added, the solvents are removed in vacuo, and the residue is chromatographed, giving 67.9 mg (58.6%) of 2-amino-6-chloro-4-[3-(5-aminopentyloxy)phenyl]quinazoline (“A141”), MW 357.86.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947696B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-836ab213356d4344832f811eae7761e0 |
| Source note | uspto-grants-2011_05 |