Hydrochloric Acid → (R)-3-amino-1-carbomethoxymethyl-3,4-dihydrocarbostyril hydrochloride

HRID 1828338

Reaktionsgleichung

Reaktionsgleichung von HRID 1828338
C(OC([NH:8][C@@H:9]1[CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:19][C:20]([O:22][CH3:23])=[O:21])[C:10]1=[O:24])=O)(C)(C)C.[ClH:25]>O1CCOCC1>[ClH:25].[NH2:8][C@@H:9]1[CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:19][C:20]([O:22][CH3:23])=[O:21])[C:10]1=[O:24]

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 69194872(R)-3-t-butyloxycarbonylamino-1-carbomethoxymethyl-3,4-dihydrocarbostyril

Produkt 1

HCID 69197166(R)-3-amino-1-carbomethoxymethyl-3,4-dihydrocarbostyril hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

(R)-3-t-butyloxycarbonylamino-1-carbomethoxymethyl-3,4-dihydrocarbostyril (20 mg) was dissolved in 4 M hydrogen chloride in 1,4-dioxane solution (5 mL) at room temperature. After 1 h the solvent was evaporated under vacuum, and the residue was twice taken up in toluene (10 mL) and evaporated under vacuum to provide (R)-3-amino-1-carbomethoxymethyl-3,4-dihydrocarbostyril hydrochloride, a white solid (21 mg).

Aufarbeitung

  1. customAfter 1 h the solvent was evaporated under vacuum
  2. customevaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-56c3882b1b994e8d9efe794ceb1eef56
Quelldatensatz
uspto-grants-2006_06
Patentnummer
US07057046B2

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