HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270314Generated: November 1, 2026
Acetaldehyde → 4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]-N,N-diethylaniline
https://huagongshe.com/reaction/1270314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 12095702 | HCID 12095702 | — |
| Product | 4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]-N,N-diethylaniline | HCID 18449106 | — |
Reaction Steps
10 mg (0.08 mmol) of sodium cyanoborohydride and 10 mg (0.17 mmol) of acetaldehyde are added to a solution of 40 mg (0.08 mmol) of 4-[5,7-dimethyl-4-(3,4,5-trimethoxyphenoxy)imidazo[5,1-f][1,2,4]triazin-2-yl]aniline from example 1 in methanol and the mixture is stirred at 20° C. After expiration of the reaction time, the mixture is treated with 2N hydrochloric acid. The methanol is removed under reduced pressure and the aqueous residue is washed with dichloromethane, rendered alkaline using sodium hydroxide, and extracted twice with dichloromethane. The organic phase is dried over sodium sulfate and purified by chromatography (eluent:dichloromethane/methanol 80:1-60:1-40:1 plus a drop of NH4OH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202243B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-4a8bde4e1b044c9fbc9d6f89afadb3f7 |
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| Source note | uspto-grants-2007_04 |
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