HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226640Generated: October 31, 2026
HCID 15289396, compound → HCID 15289397, compound
https://huagongshe.com/reaction/2226640
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 15289396 | HCID 15289396 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 15289397 | HCID 15289397 | — |
Reaction Steps
In a first embodiment, a novel bifunctional compound was prepared by first reacting methoxycarbonylsulfenyl chloride with 2-aminoethanethiol hydrochloride, then 2-mercaptopyridine to form 2-[(2-pyridinyl)dithio]ethanamine hydrochloride (see FIG. 2). This compound was then reacted with phosgene in the presence of triethylamine (TEA), then t-butyl carbazate, to form N-[2-[(2-pyridinyl)dithio]ethyl]-2-(tert.-butoxy-carbonyl)hydrazinecarboxamide. The hydrazinecarboxamide was next dissolved in TFA to form N-[2-[(2-pyridinyl)dithio]ethyl]hydrazinecarboxamide, compound 10, a semicarbazide, which was then reacted with adriamycin hydrochloride to form the semicarbazone derivative of ADM containing a reactive pyridinyldithio moiety, compound 1, FIG. 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05349066 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-29cf81c19ce74c04811e27f354382eaa |
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| Source note | uspto-grants-1994_09 |
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