Sodium hydride → HCID 58409942, Verbindung

HRID 1844877Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1844877
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1O[C:15](=O)[C:14]([C:18]#[N:19])=[C:13]([N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[CH:12]=1.[H-].[Na+]>C1COCC1>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1[C:12]2[CH2:11][C:2]3[C:1](=[CH:10][CH:5]=[CH:4][CH:3]=3)[C:15]=2[C:14]([C:18]#[N:19])=[C:13]([N:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[CH:12]=1

Komponenten

4

Versuchsvorschrift

A mixture of 6-(naphthalen-2-yl)-2-oxo-4-(piperidin-1-yl)-2H-pyran-3-carbonitrile (330 mg), indanone-1 (132 mg) and NaH (39 mg) in THF was stirred for <5 min. After completion, the reaction solvent was evaporated under vacuum to dryness and crude, solid was quenched with ice water and subsequently neutralized with dil. HCl, finally purified by column chromatography using ethylacetate-hexane as eluent. White solid; mp 136-138° C.; ESIMS 401 (M++1); IR (KBr) 2214 cm−1 (CN); HRMS calcd. for C2H24N2 400.1940 Found 400.1939.

Aufarbeitung

  1. customAfter completion, the reaction solvent was evaporated under vacuum to dryness and crude, solid
  2. customwas quenched with ice water
  3. customfinally purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-09ab6418a39d4d54b008c011ecc69b57
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08946682B2

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