Reaktion #342525

ord-113c25239d61448faf92cc47a1cf30db

Reaktionsgleichung

NC1CCN(CCn2c(=O)cnc3ccc(F)cc32)CC1
1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one
NC1CCN(CCn2c(=O)cnc3ccc(F)cc32)CC1
Intermediate 140
NC1CCN(CCn2c(=O)cnc3ccc(F)cc32)CC1
1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one
O=C(O)c1cc2cc(F)ccc2[nH]1
5-fluoro-1H-indole-2-carboxylic acid
CC[N+](=C=N)CCCN(C)C
N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide
O.On1nnc2ccccc21
1-Hydroxybenzotriazole hydrate
O=C(NC1CCN(CCn2c(=O)cnc3ccc(F)cc32)CC1)c1cc2cc(F)ccc2[nH]1
title compound
Ausbeute 79.6%
O=C(NC1CCN(CCn2c(=O)cnc3ccc(F)cc32)CC1)c1cc2cc(F)ccc2[nH]1
5-Fluoro-N-{1-[2-(7-fluoro-2-oxoquinoxalin-1(2H)-yl)ethyl]piperidin-4-yl}-1H-indole-2-carboxamide
Ausbeute 79.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed under reduced pressure
  2. 2
    workup.STIRRINGstirred for 45 minutes
  3. 3
    Filtrationfiltered

Vorschrift

A mixture of 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one (Intermediate 140, 130 mg, 0.448 mmol), 5-fluoro-1H-indole-2-carboxylic acid (96.3 mg, 0.538 mmol), N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide (EDC)(124 mg, 0.645 mmol) and 1-Hydroxybenzotriazole hydrate (HOBT) (87 mg, 0.645 mmol) in dichloromethane/DMF (4:1, 10 mL) was stirred for 2.5 hours at room temperature. The solvent was removed under reduced pressure and the residue was suspended in methanol, stirred for 45 minutes and then filtered to give title compound (161 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07875715B2uspto-grants-2011_01