HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622711Generated: October 26, 2026
Ethyl orthoformate → HCID 178482140, compound
https://huagongshe.com/reaction/622711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 1-(4-(3-Aminophenyl)thiazol-2-yl)guanidine | HCID 178512611 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 178482140 | HCID 178482140 | — |
Reaction Steps
A mixture of 9.3 g (0.04 mole) of 3-(2-guanidino-4-thiazolyl)benzeneamine, 20 ml of triethylorthoformate, and 2 drops of trifluoroacetic acid is stirred at reflux for 5 hours after which it is concentrated in vacuo. The residue is dissolved in 20 ml of ethanol, the solution cooled to 0° C. and then treated with excess sodium borohydride. The mixture is allowed to warm to room temperature, then stirred at reflux for 4 hours. Upon concentration in vacuo the residue is partitioned between water and dichloromethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04772622 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-bf26f55371854a828c4f5bb935c679d5 |
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| Source note | uspto-grants-1988_09 |
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