HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 21098395, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 21098394 | HCID 21098394 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21098395 | HCID 21098395 | — |
Reaction Steps
To a solution of (6,7-dimethoxy-5-nitro-quinazolin-4-yl)-phenyl-amine (1.0 g, 3.14 mmol) (from Example 1, Step B, supra), NH4Cl (1.7 g, 31.4 mmol) in MeOH, H2O and CHCl3 (40 mL, 2:1:1) was added Zn powder (2.0 g, 31.4 mmol) (Aldrich). The reaction mixture was stirred at room temperature for 1 hour. The mixture was then filtered, the filtrate was concentrated and then extracted with chloroform (100 mL). The organic layer was separated, dried over Na2SO4, and concentrated. The residue was purified by chromatography using EtOAc/CH2Cl2 (1:1) as eluent to give the desired 6,7-dimethoxy-N 4-phenyl-quinazoline-4,5-diamine as a yellow gum. (Yield 0.5 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217717B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-cfb297ba46c74180bd001681bce3c97a |
| Source note | uspto-grants-2007_05 |