Sodium Acetate → HCID 178446964, compound

HRID 1297726Notes

Reaction equation

HRID 1297726 reaction equation
[CH3:1][C:2]([CH3:20])([CH3:19])[CH2:3][O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([CH:15]=O)[CH:13]=2)[N:8]=[CH:7][C:6]=1[C:17]#[N:18].[CH:21]1([NH:24][C:25]2[S:26][CH2:27][C:28](=[O:30])[N:29]=2)[CH2:23][CH2:22]1.C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH:21]1([NH:24][C:25]2[S:26]/[C:27](=[CH:15]\[C:12]3[CH:13]=[C:14]4[C:9](=[CH:10][CH:11]=3)[N:8]=[CH:7][C:6]([C:17]#[N:18])=[C:5]4[O:4][CH2:3][C:2]([CH3:20])([CH3:19])[CH3:1])/[C:28](=[O:30])[N:29]=2)[CH2:23][CH2:22]1

Participants

5

Procedure

Similar procedure as described in example 28c was used, starting from 4-(2,2-dimethyl-propoxy)-6-formyl-quinoline-3-carbonitrile (example 67b), 2-cyclopropylamino-thiazol-4-one (example 37c), sodium acetate and acetic acid to give 6-[2-cyclopropylamino-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-4-(2,2-dimethyl-propoxy)-quinoline-3-carbonitrile. LC-MS m/e 407 (MH+).

Sources & evidence

ORD record
ord-57ac1053c45d4f8a81996e252fa8c4a0
Source dataset
uspto-grants-2007_07
Patent number
US07250515B2

Reaction notes

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