HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461334Generated: October 30, 2026
Hydrochloric Acid → 4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)piperazine-1-imidic Acid Methyl Ester
https://huagongshe.com/reaction/461334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-Cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline | HCID 21393366 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Amino-6,7-dimethoxyquinazolin-2-yl)piperazine-1-imidic Acid Methyl Ester | HCID 54091059 | — |
Reaction Steps
Under anhydrous conditions, 6.3 g. (0.02 mole) of 2-(4-cyanopiperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline is dissolved in 150 ml. of ethyl ether and 1.8 ml. (0.044 mole) of reagent grade methanol is added. The solution is cooled to 0° C. and anhydrous hydrogen chloride is added until the solution is acid to Congo red paper. The resulting mixture is stored at 0° C. for 2 hours, then allowed to warm to room temperature (25° C) overnight. The reaction mixture is made alkaline with 2N sodium hydroxide, the ether layer separated, washed with 2 × 50 ml. of water, dried over anhydrous magnesium sulfate and evaporated to dryness to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04062844 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-bfb94a40fcda490093ddddb33ba7879b |
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| Source note | uspto-grants-1977_12 |
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