Isonicotinic Acid → HCID 90047361, compound

HRID 1507589Notes

Reaction equation

HRID 1507589 reaction equation
[NH2:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]3([CH2:16][CH2:15]3)[C:7](=[O:14])[N:8]2[CH:11]2[CH2:13][CH2:12]2)=[CH:4][CH:3]=1.[C:17](O)(=[O:24])[C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1>>[CH:11]1([N:8]2[C:9]3[C:5](=[CH:4][CH:3]=[C:2]([NH:1][C:17](=[O:24])[C:18]4[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=4)[CH:10]=3)[C:6]3([CH2:16][CH2:15]3)[C:7]2=[O:14])[CH2:12][CH2:13]1

Participants

3

Reactant 2

HCID 5922Isonicotinic AcidHCID 118415186HCID 118415186, compound

Product 1

HCID 90047361HCID 90047361, compound

Procedure

Prepared in analogy to example 26 from 6′-amino-1′-cyclopropylspiro[cyclopropane-1,3′-indolin]-2′-one and isonicotinic acid. The title compound was obtained as light yellow crystals.

Sources & evidence

ORD record
ord-4aef5491769a4a4a807d59a085115c71
Source dataset
uspto-grants-2015_12
Patent number
US09221816B2

Reaction notes

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