HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178492025, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68285181 | HCID 68285181 | — |
| Product | HCID 178492025 | HCID 178492025 | — |
Reaction Steps
Diphenyl cyano carbonimidate (3.48 mmol) was added to a solution of 6-bromo-N4-(6-methoxypyridin-3-yl)quinoline-3,4-diamine (compound of step 3, 2.90 mmol) in dry acetonitrile (10 ml), followed by the addition of di-isopropyl ethyl amine (4.35 mmol). The resulting reaction mixture was refluxed for 48 h. The reaction mixture was cooled to RT, concentrated under vacuum and purified (silica gel column, MeOH/CHCl3 as eluent) to obtain the title compound. 1H NMR (300 MHz, DMSO-d6): δ 13.81 (s, 1H), 8.96 (s, 1H), 8.53 (d, J=3 Hz, 1H), 8.10 (d, J=3 Hz, 1H), 8.06 (d, J=9 Hz, 1H), 7.80 (dd, J=9 Hz, 3 Hz, 1H), 7.20 (d, J=9 Hz, 1H), 7.13 (d, J=3 Hz, 1H), 4.00 (s, 3H); MS (m/z): 395 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062046B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-cd2a19f9f7a0412b81d07720acdb3060 |
| Source note | uspto-grants-2015_06 |