HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, 1-ethoxy-4-isocyanato- → HCID 58770687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, 1-ethoxy-4-isocyanato- | HCID 122887 | — |
| Reactant | 6,7-Dimethoxy-4-(piperidin-4-yl)quinazoline | HCID 59551734 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58770687 | HCID 58770687 | 20.2% |
Reaction Steps
A solution of 6,7-dimethoxy-4-piperidin-4-yl-quinazoline (30 mg, 0.110 mmol), as prepared in Example 1d, in DMF (1 mL) was treated with 1-ethoxy-4-isocyanato-benzene (26.8 mg, 0.164 mmol) at RT overnight. The reaction was then partitioned between EtOAc (10 mL) and H2O (10 mL). The organic phase was dried over Na2SO4 and concentrated in vacuo. Purification by prep tlc (1:9 MeOH/DCM) afforded the title compound as a light brown solid (9.7 mg, 20%). 1H NMR (300 MHz, CDCl3) δ 9.09 (s, 1H), 7.41 (m, 1H), 7.26 (m, 3H), 6.87 (m, 2H), 6.29 (br s, NH), 4.30-4.25 (m, 2H), 4.08 (s, 6H), 4.01 (q, 2H), 3.61 (m, 1H), 3.17 (m, 2H), 2.17 (m, 2H), 2.02-2.01 (m, 2H), 1.40 (t, 3H); LC/MS (ESI): calcd mass 436.2, found 437.3 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071768B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-02093f1c0747459889151d794c573b8b |
| Source note | uspto-grants-2011_12 |