Sodium Acetate → 6-(4-Oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-4-pyridin-3-yl-quinoline-3-carbonitrile

HRID 1297713Notes

Reaction equation

HRID 1297713 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][C:7]([C:13]#[N:14])=[C:6]2[C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)=O.[S:21]1[CH2:27][C:25](=[O:26])[NH:24][C:22]1=[S:23].C([O-])(=O)C.[Na+]>C(O)(=O)C>[O:26]=[C:25]1[C:27](=[CH:1][C:3]2[CH:4]=[C:5]3[C:10](=[CH:11][CH:12]=2)[N:9]=[CH:8][C:7]([C:13]#[N:14])=[C:6]3[C:15]2[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=2)[S:21][C:22](=[S:23])[NH:24]1

Participants

5

Procedure

Similar procedure as described in example 61j was used, starting from 6-formyl-4-pyridin-3-yl-quinoline-3-carbonitrile (example 63c), rhodanine, sodium acetate, and acetic acid to give 6-(4-oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-4-pyridin-3-yl-quinoline-3-carbonitrile. LC-MS m/e 375 (MH+).

Sources & evidence

ORD record
ord-63945e74924a459a81227e876e7fe444
Source dataset
uspto-grants-2007_07
Patent number
US07250515B2

Reaction notes

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