HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → HCID 21936064, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | HCID 21935986 | HCID 21935986 | — |
| Product | HCID 21936064 | HCID 21936064 | — |
Reaction Steps
Using an analogous procedure to that described in Example 12, 4-(6-chloro-2,3-methylenedioxyanilino)-6-methoxy-7-(piperidin-4-ylmethoxy)quinazoline was reacted with 2-chloroacetonitrile to give the title compound as a solid; NMR Spectrum: (DMSOd6) 1.65 (m, 2H), 2.1 (m, 2H), 2.2 (m, 1H), 3.15 (m, 2H), 3.6 (m, 2H), 4.05 (s, 3H), 4.15 (m, 2H), 4.55 (s, 2H), 6.15 (s, 2H), 7.05 (d, 1H), 7.15 (d, 1H), 7.4 (s, 1H), 8.15 (s, 1H), 8.9 (s, 1H); Mass Spectrum: M−H− 480 and 482.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115615B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-d98ee673e4af43c281267a6c3509684f |
| Source note | uspto-grants-2006_10 |