HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-5-tert-butylselenophene-2-carboxamide → HCID 86698308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-5-tert-butylselenophene-2-carboxamide | HCID 86646889 | — |
| Reactant | DMF NaOH | HCID 86698281 | — |
| Reactant | HCID 86698307 | HCID 86698307 | — |
| Product | HCID 86698308 | HCID 86698308 | — |
Reaction Steps
The reaction of 6-(3-morpholinopropoxy)-4-chloro-7-methoxy-2-methylquinazoline with 3-amino-5-tert-butylselenophene-2-carboxamide in the presence of DMF/NaOH as described in Example 1 gave title compound as a brown color solid, mp 204-206° C. 1H NMR (400 MHz, CDCl3): δ 11.92 (1H, br s), 8.95 (1H, s), 7.34 (1H, s), 7.18 (1H, s), 5.37 (2H, br s), 4.29 (2H, t, J=6.0 Hz), 3.98 (3H, s), 3.73 (4H, t, J=4.4 Hz), 2.70 (3H, s), 2.61 (2H, t, J=7.2 Hz), 2.50 (4H, br s), 2.11-2.14 (2H, m), 1.47 (9H, s); LC-MS (positive ion mode): m/z 560, 562 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815879B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1589b5bc970d43d093f0219b46b9d262 |
| Source note | uspto-grants-2014_08 |