HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinazolinedione → HCID 68388750, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinazolinedione | HCID 64048 | — |
| Reactant | 1-(2-Pyrimidinyl)piperazine | HCID 88747 | — |
| Reactant | Methyl 3-(2-bromoethyl)benzoate | HCID 10586288 | — |
| Reactant | HCID 68388719 | HCID 68388719 | — |
| Product | HCID 68388750 | HCID 68388750 | — |
Reaction Steps
The compound was prepared from 1-(3-carboxyphenethyl)quinazoline-2,4(1H,3H)-dione (prepared from quinazoline-2,4(1H,3H)-dione and methyl 3-(2-bromoethyl)benzoate using a procedure similar to those used for Examples 1 and 2) and 2-(piperazin-1-yl)pyrimidine using a procedure similar to those described for the synthesis of compound of Example 3. 1H NMR (DMSO-d6): 11.54 (s, 1H), 8.37 (d, J=4.8 Hz, 2H), 7.78 (dd, J=7.8 and 1.5 Hz, 1H), 7.73 (t, J=6.9 Hz, 1H), 7.52 (d, J=7.2 Hz, 1H), 7.35-7.22 (m, 5H), 6.66 (t, J=4.7 Hz, 1H), 4.28 (t, J=7.5 Hz, 2H), 3.80-3.20 (m, 8H), 2.95 (t, J=7.4 Hz, 1H). MS: m/z 457.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290460B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-007a42198f364dec879a0027655473d5 |
| Source note | uspto-grants-2016_03 |