Hydrochloric Acid → [6-(3-Chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yl]-(3,3-dimethyl-2,3-dihydro-1H-indol-6-yl)-amine HCl salt

HRID 535370Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 535370
[Cl:1][C:2]1[C:3]([N:8]2[CH2:32][CH2:31][C:11]3[N:12]=[CH:13][N:14]=[C:15]([NH:16][C:17]4[CH:25]=[C:24]5[C:20]([C:21]([CH3:30])([CH3:29])[CH2:22][N:23]5C(=O)C)=[CH:19][CH:18]=4)[C:10]=3[CH2:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1.Cl>CCO>[ClH:1].[Cl:1][C:2]1[C:3]([N:8]2[CH2:32][CH2:31][C:11]3[N:12]=[CH:13][N:14]=[C:15]([NH:16][C:17]4[CH:25]=[C:24]5[C:20]([C:21]([CH3:29])([CH3:30])[CH2:22][NH:23]5)=[CH:19][CH:18]=4)[C:10]=3[CH2:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

A mixture of 1-{6-[6-(3-chloro-pyridin-2-yl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-ylamino]-3,3-dimethyl-2,3-dihydro-indol-1-yl}-ethanone (30 mg), EtOH (5 mL), and 5N aqueous HCl (1 mL) was stirred at 55° C. for 10 h. The mixture was concentrated in vacue to give the HCl salt as a light yellow solid (35 mg).

Aufarbeitung

  1. concentrationThe mixture was concentrated in vacue

Quellen und Nachweise

ORD-Eintrag
ord-4ab256243ee34676be7f283167ec7999
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08859545B2

Notizen zur Reaktion

Wird geladen…