HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976113Generated: October 29, 2026
HCID 14115670, compound → HCID 178437163, compound
https://huagongshe.com/reaction/1976113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14115670 | HCID 14115670 | — |
| Reactant | HCID 178430658 | HCID 178430658 | — |
| Reactant | HCID 178465517 | HCID 178465517 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178437163 | HCID 178437163 | — |
Reaction Steps
7-[N2,N3-Bis(benzyloxycarbonyl)guanidino]-8-methylquinoline. To a pale yellow solution of 500 mg of 7-amino-8-methylquinoline in 20 mL of tetrahydrofuran are added 1.18 g of ethyl N,N-bis(benzyloxy-carbonyl)pseudothiourea and 1.01 g of mercuric acetate and the mixture is stirred at room temperature for 1 hour. The suspension is diluted with ethyl acetate and the organic layer is washed with water followed by brine. The aqueous layers are extracted with ethyl acetate; the combined organic layers are dried over magnesium sulfate, filtered and rotary evaporated. The residue is purified by flash column chromatography on silica gel, eluting with 50% ethyl acetate/hexanes and recrystallization from hexanes/methylene chloride to provide 1.257 g of 7-[N2,N3-bis(benzyloxycarbonyl)guanidino]-8-ethylquinoline as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06225331B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-657acd9daa804767863a5934dd8ca44e |
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| Source note | uspto-grants-2001_05 |
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