HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(6,7-Dimethoxyquinazolin-4-ylthio)aniline → HCID 58267839, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(6,7-Dimethoxyquinazolin-4-ylthio)aniline | HCID 56953627 | — |
| Reactant | HCID 59394199 | HCID 59394199 | — |
| Product | HCID 58267839 | HCID 58267839 | 69% |
Reaction Steps
The title compound was prepared using the procedure described in Example 113C with 3-(6,7-dimethoxyquinazolin-4-ylthio)aniline described in Example 115B (94 mg, 0.3 mmol) and phenyl 5-isopropylisoxazol-3-ylcarbamate described in Example 133A (110 mg, 0.45 mmol). Precipitation of the desired product detected completion of reaction. The solid was filtered off and washed with diethyl ether to give 1-(3-(6,7-dimethoxyquinazolin-4-ylthio)phenyl)-3-(5-isopropylisoxazol-3-yl)urea (96.26 mg, 69%) as a solid. 1H NMR (300 MHz, DMSO-d6) δ 9.57 (s, 1H), 9.02 (s, 1H), 8.70 (s, 1H), 7.84 (s, 1H), 7.53-7.42 (m, 2H), 7.36-7.27 (m, 3H), 6.51 (s, 1H), 3.99 (s, 6H), 3.04-3.00 (m, 1H), 1.23 (d, 6H); LC-MS (ESI) m/z 466 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09320739B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c70cdef783ec4957b4ee5fe58c25e1fb |
| Source note | uspto-grants-2016_04 |