HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 67024743, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54163752 | HCID 54163752 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67024743 | HCID 67024743 | — |
Reaction Steps
47 μl of acetic anhydride and catalytic amounts of 4-dimethyl-aminopyridine are added to 250 mg of 4-[(3-chloro-4-fluorophenyl)amino]-6-[(4-{N-[(ethoxycarbonyl)methyl]-N-(2-hydroxyethyl)amino}-1-oxo-2-buten-1-yl)amino]-7-cyclopropylmethoxy-quinazoline in 2 ml of methylene chloride. The reaction mixture is stirred overnight at ambient temperatures and then evaporated to dryness. The crude product is purified by chromatography on a silica gel column with methylene chloride, followed by methylene chloride/methanol (9:1) as eluant. Yield: 150 mg (56% of theory), Melting point: 90-92° C. Mass spectrum (ESI+): m/z=614, 616 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972288B1 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-62abaf3219d4485aa739e382fccf5773 |
| Source note | uspto-grants-2005_12 |