HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethylisoxazol-5-amine → HCID 66907111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethylisoxazol-5-amine | HCID 10866295 | — |
| Reactant | HCID 86238128 | HCID 86238128 | — |
| Product | HCID 66907111 | HCID 66907111 | 55% |
Reaction Steps
Using an analogous procedure to that described in Example 19, 2-[4-(6,7-dimethoxyquinazolin-4-yloxy)phenyl]acetyl chloride was reacted with 5-amino-3-ethylisoxazole. There was thus obtained the title compound in 55% yield; 1H NMR: (DMSOd6) 1.16 (t, 3H), 2.56 (q, 2H), 3.76 (s, 2H), 3.97 (s, 3H), 3.99 (s, 3H) 6.16 (s, 1H), 7.27 (d, 1H), 7.39 (s, 1H), 7.41 (d, 2H), 7.55 (s, 1H), 8.54 (s, 1H); Mass Spectrum: M+H+ 435.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153643B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c5dc829a8da046498a5e8d775787250d |
| Source note | uspto-grants-2012_04 |