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HRID 2425412Erstellt: 27. Oktober 2026

3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine → Hydrochloric Acid

https://huagongshe.com/reaction/2425412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidineHCID 2761404—
Edukt(S)-Methyl-pyrrolidin-3-yl-carbamic acid tert-butyl esterHCID 7171888—
Edukt5-Isoquinolinesulfonyl chloride,1,4-dichloro-HCID 76851489—
Edukt5-Isoquinolinesulfonyl chloride,4-bromo-1-chloro-HCID 76851490—
Edukt3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(1,4-dichloro-5-isoquinolinesulfonyl)pyrrolidineHCID 86627812—
ProduktHydrochloric AcidHCID 313—
ProduktHCID 178482264HCID 178482264—

Reaktionsschritte

3-[N-(tert-Butoxycarbonyl)-N-methylamino]-1-(1,4-dichloro-5-isoquinolinesulfonyl)pyrrolidine (Intermediate 25) can be prepared by using 1,4-dichloro-5-isoquinolinesulfonyl chloride and 3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine in the method of Example 35-1, Step A instead of 1-chloro-4-bromo-5-isoquinolinesulfonyl chloride and (S)-3-[N-(tert-butoxycarbonyl)-N-methylamino]pyrrolidine, respectively, and then used in the method of Example 35-1, Step B in a similar manner to obtain the title compound as hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07964613B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-decfa694efea455baa131f5a484d72a8
Quellennotizuspto-grants-2011_06