HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164228Generated: November 1, 2026
Chloroacetaldehyde → HCID 13394199, compound
https://huagongshe.com/reaction/2164228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 2,6-Dimethoxy-4-aminopyrimidine | HCID 76789 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13394199 | HCID 13394199 | — |
Reaction Steps
A mixture of 1.5 g (0.01 mole) of 4-amino-2,6-dimethoxypyrimidine and 3.0 g (0.015 mole) of 50% aqueous chloroacetaldehyde in 20 ml of water was heated at 80° C. for one hour, and was then cooled with an ice bath with concomitant neutralization with sodium bicarbonate. The solid which formed was separated by filtration and recrystallized from cyclohexane with treatment with decolorizing charcoal. White crystals of 5,7-dimethoxyimidazo[1,2-c]pyrimidine, m.p. 120°-121° C., were obtained. Analysis: Calculated for C8H9N3O2 : %C,53.6; %H,5.1; %N,23.5; Found: %C,53.5; %H,5.0; %N,23.6. The structural assignment was confirmed by infrared and nuclear magnetic resonance spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04503050 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-9e3a9064dfa24fe1bfe3e6f65c3ce100 |
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| Source note | uspto-grants-1985_03 |
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