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HRID 1059469Erstellt: 25. Oktober 2026

Alpha-Cyano-4-Hydroxycinnamic Acid → HCID 178429055, Verbindung

https://huagongshe.com/reaction/1059469

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAlpha-Cyano-4-Hydroxycinnamic AcidHCID 2102—
Edukt5-methyl-3-[(2-(N-methyl-N-(3-pyridylmethyl)aminosulfonyl) phenylsulfonyloxy]phenoxy]propoxyamineHCID 86589072—
EduktHCID 178427271HCID 178427271—
ProduktHCID 178429055HCID 17842905576%

Reaktionsschritte

3-[5-Methyl-3-[(2-(N-methyl-N-(3-pyridylmethyl)aminosulfonyl)phenylsulfonyloxy]phenoxy]propoxy guanidine dihydrochloride: The title compound was prepared in 76% yield from 3-[5-methyl-3-[(2-(N-methyl-N-(3-pyridylmethyl)aminosulfonyl) phenylsulfonyloxy]phenoxy]propoxyamine, as prepared in the preceding step, in a manner analogous to step f of Example 1. 1H-NMR (300 MHz, DMSO-d6) δ 8.78 (t, J=5.2 Hz, 2H), 8.23 (m, 3H), 8.06 (t, J=7.7 Hz, 1H), 7.94 (t, J=7.7 Hz, 1H), 7.88 (t, J=7.9 Hz, 1H), 7.71 (br s, 4H), 6.75 (s, 1H), 6.55 (s, 1H), 6.51 (s, 1H), 4.72 (s, 2H), 3.99 (t, J=6.3 Hz, 2H), 3.90 (t, J=6.4 Hz, 2H), 2.88 (s, 3H), 2.22 (s, 3H), 2.01 (pentet, J=6.4 Hz, 2H). Mass spectrum (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C24H29N5O7S2: 564.2 (M+H), 586.1 (M+Na). Found: 564.1, 586.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06518310B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-d97726bf848a4f9bbedfa529ee2c48b4
Quellennotizuspto-grants-2003_02