HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248089Generated: October 30, 2026
Ammonium Hydroxide → HCID 14700378, compound
https://huagongshe.com/reaction/2248089
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Methanol, 1,1-diethoxy-, 1-acetate | HCID 84166 | — |
| Reactant | HCID 14986942 | HCID 14986942 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14700378 | HCID 14700378 | — |
Reaction Steps
2-[(3-Amino-4-quinolinyl)amino]-1-propanol (0.113 mole) as a crude reaction product obtained by the method of Example 4, was mixed with a 20 percent molar excess of diethoxymethyl acetate (22.3g, 0.136 mole) and heated for 0.75 hour. To the mixture was added 150 mL of water. The resulting mixture was made basic with concentrated ammonium hydroxide, and extracted first with ethyl acetate, then with chloroform. The extracts were combined, dried over magnesium sulfate, and evaporated, slurried in 1:1 chloroform/diethyl ether and separated by filtration to provide the solid product, beta-methyl-1H-imidazo[4,5-c]-quinoline-1-ethanol, m.p. 170°-174° C. after recrystallization from ethanol with treatment with decolorizing carbon. Analysis: Calculated for C13H13N3O: %C, 68.7; %H, 5.8; %N, 18.5; Found: %C, 68.5; %H, 5.8; %N, 18.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037986 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-7a6d09978edd4c95913defbd79947335 |
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| Source note | uspto-grants-1991_08 |
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