HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412000Generated: October 29, 2026
HCID 18535765, compound → HCID 18535766, compound
https://huagongshe.com/reaction/412000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18535765 | HCID 18535765 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 18535766 | HCID 18535766 | 83.3% |
Reaction Steps
A solution of 6-amino-4-(4-benzyloxyanilino)quinazoline hydrochloride (1.46 g, 3.57 mmol) in methanol/THF (1:1, 100 mL) was hydrogenated over Raney nickel (1 g) at 51.5 psi and 23° C. for 18 hours. The reaction mixture was celite filtered, and the volatiles were removed under reduced pressure. The crystalline brown residue was partially redissolved in MeOH (25 mL), and dilute aqueous Na2CO3 solution (0.1 M, 50 mL) was added with vigourous stirring. After 2 hours, the precipitate was collected by Buchner filtration, rinsed with water (50 mL), dried in a vacuum oven at 60° C., and then purified by flash chromatography on silica gel, eluting with CHCl3 then 4% MeOH in CHCl3 to give 6-amino-4-(4-benzyloxyanilino)quinazoline (1.018 g, 80%) as a cream powder; mp 173-175° C., remelt 240-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562818B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-b0f8d0fe20f04d568eaf507e5131253a |
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| Source note | uspto-grants-2003_05 |
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