HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-((3-Chloro-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol → HCID 68523549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-((3-Chloro-2-fluorophenyl)amino)-7-methoxyquinazolin-6-ol | HCID 57476868 | — |
| Reactant | HCID 86600825 | HCID 86600825 | — |
| Product | HCID 68523549 | HCID 68523549 | 95% |
Reaction Steps
4-(3-chloro-2-fluoroanilino)-6-hydroxy-7-methoxyquinazoline was reacted with tert-butyl (3R)-3-[(4-nitrophenyl)sulfonyloxy]pyrrolidine-1-carboxylate to give 4-(3-chloro-2-fluoroanilino)-6-[(3S)-1-(tert-butoxycarbonyl)pyrrolidin-3-yloxy]-7-methoxyquinazoline as a dry foam (2.9 g, 95%); 1H NMR Spectrum: (DMSO d6) 1.40 (s, 9H); 2.07-2.29 (m, 21-1); 3.32-3.50 (m, 3H); 3.64-3.70 (dd, 1H); 3.92 (s, 3H); 5.08-5.18 (m, 1H); 7.21 (s, 1H); 7.23-7.30 (m, 1H); 7.43-7.55 (m, 2H); 7.79 (s, 1H); 8.36 (s, 1H); 9.6 (s, 1H); Mass Spectrum: (M+H)+ 489.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399667B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-dc7fb8bc159843c1880f95c77aa1d14b |
| Source note | uspto-grants-2013_03 |