HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491496Generated: October 31, 2026
Guanidine Hydrochloride → HCID 57678441, compound
https://huagongshe.com/reaction/491496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Benzenamine hydrochloride (1:1) | HCID 8870 | — |
| Reactant | HCID 68839019 | HCID 68839019 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57678441 | HCID 57678441 | 36.7% |
Reaction Steps
2-(2,5-Diiodo-4-methoxy-phenoxy)-but-2-enenitrile (3.47 g, 6.75 mmol) and aniline hydrochloride (3.5 g, 27 mmol) were dissolved in 27 mL ethanol. The reaction mixture was heated to 85° C. and stirred under nitrogen for 18 hours. The reaction mixture was cooled and 25% NaOCH3 in methanol (7.3 mL) was added, followed by guanidine hydrochloride (3.2 g), and ethanol (10 mL). The reaction mixture was heated to 100° C. for 21 hours, then cooled and concentrated under reduced pressure. The residue was poured into water and extracted with dichloromethane. The combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure to give 1.2 g of 5-(2,5-Diiodo-4-methoxy-phenoxy)-pyrimidine-2,4-diamine, MS (M+H)=485.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531547B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-c8a6a9147aa74e76860095c949d126ca |
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| Source note | uspto-grants-2009_05 |
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