HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(4-Chloro-3-formamidobenzyl)amino-6-chloroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(3-Amino-4-chlorobenzyl)amino-6-chloroquinazoline | HCID 18796713 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4-(4-Chloro-3-formamidobenzyl)amino-6-chloroquinazoline | HCID 18796669 | — |
Reaction Steps
0.90 g (2.82 mmol) of the 4-(3-amino-4-chlorobenzyl)amino-6-chloroquinazoline prepared in Example 151 was dissolved in 15 ml of formic acid, followed by the addition of 1 ml of acetic anhydride. The obtained mixture was stirred at room temperature for several hours and distilled under a reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (ethyl acetate) and recrystallized from ethyl acetate to give 0.64 g of the title compound as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05801180 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-ac7b2af71c5a4b89a2d47ddaf306111b |
| Source note | uspto-grants-1998_09 |