HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(6-Methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)aniline → HCID 58267893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(6-Methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)aniline | HCID 66876764 | — |
| Reactant | Phenyl 3-(2-cyanopropan-2-yl)phenylcarbamate | HCID 66877200 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58267893 | HCID 58267893 | 23% |
Reaction Steps
Using the procedure described in Example 278B, to a solution of 3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)aniline (102 mg, 0.3 mmol), prepared as described in Example 230A, in THF (3 ml) was added DMAP (18 mg, 0.15 mmol) and phenyl 3-(2-cyanopropan-2-yl)phenylcarbamate (92 mg, 0.33 mmol) described in Example 278A to afford 1-(3-(2-cyanopropan-2-yl)phenyl)-3-(3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)phenyl)urea (37.2 mg, 23%) as a solid. 1H NMR (300 MHz, DMSO-d6) δ 1.67 (s, 6H), 3.76 (s, 3H), 4.00 (s, 4H), 4.34 (s, 3H), 7.11 (d, J=6 Hz, 1H), 7.24-7.43 (m, 7H), 7.66 (s, 1H), 7.84 (s, 1H), 8.69 (s, 1H), 8.92 (d, J=9 Hz, 2H); LC-MS (ESI) m/z 544 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09320739B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-ce2b7acd19694c4d8190f8974b491a0e |
| Source note | uspto-grants-2016_04 |