Triethylamine → HCID 73703361, Verbindung

HRID 2307467Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2307467
[F:1][C:2]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:3]=1[CH:4]=[CH:5][C:6]([OH:8])=O.[NH2:14][CH:15]([C:17]1[CH:18]=[C:19]2[C:23](=[CH:24][CH:25]=1)[N:22]([C:26]([O:28][CH3:29])=[O:27])[CH2:21][CH2:20]2)[CH3:16].CCN=C=NCCCN(C)C.Cl.C(N(CC)CC)C>CN(C1C=CN=CC=1)C.C(Cl)Cl.O>[F:1][C:2]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:3]=1[CH:4]=[CH:5][C:6]([NH:14][CH:15]([C:17]1[CH:18]=[C:19]2[C:23](=[CH:24][CH:25]=1)[N:22]([C:26]([O:28][CH3:29])=[O:27])[CH2:21][CH2:20]2)[CH3:16])=[O:8]

Komponenten

8

Versuchsvorschrift

A mixture of 2,4-difluorocinnamic acid (0.5 mmol), (±)-5-(1-aminoethyl)-2,3-dihydro-indole-1-carboxylic acid, methyl ester, Preparation 20 (132 mg, 0.6 mmole), EDC hydrochloride (192 mg, 1.0 mmole), DMAP (61 mg, 0.5 mmole), and triethylamine (202 mg, 2 mmole) in CH2Cl2 (8 mL) was stirred at room temperature for 16 hours. Water was added, the aqueous layer was extracted with dichloromethane, and the combined organic layers were washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The crude product was purified by flash column chromatography on silica eluting with EtOAc/hexane (7:3) to give the title compound (125 mg) as a solid.

Aufarbeitung

  1. extractionthe aqueous layer was extracted with dichloromethane
  2. washthe combined organic layers were washed with brine
  3. dry with materialdried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe crude product was purified by flash column chromatography on silica eluting with EtOAc/hexane (7:3)

Quellen und Nachweise

ORD-Eintrag
ord-d1f975ccace542029cab822285812264
Quelldatensatz
uspto-grants-2004_12
Patentnummer
US06831080B2

Notizen zur Reaktion

Wird geladen…