Ammonia → HCID 86744023, compound

HRID 2107161Notes

Reaction equation

HRID 2107161 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:9][C:10](=[O:24])[NH:11][C:12]2[S:13][CH:14]=[C:15]([C:17](=O)[C:18]([O:20][CH2:21][CH3:22])=[O:19])[N:16]=2)[CH:6]=[CH:7][CH:8]=1.[S:25]1[CH2:31][C:29](=[O:30])[N:28]([CH2:32][C:33]([OH:35])=[O:34])[C:26]1=[S:27].[Cl-].[NH4+].N>C(O)C>[OH2:2].[CH3:1][O:2][C:3]1[CH:4]=[C:5]([NH:9][C:10](=[O:24])[NH:11][C:12]2[S:13][CH:14]=[C:15]([C:17](=[C:31]3[S:25][C:26](=[S:27])[N:28]([CH2:32][C:33]([OH:35])=[O:34])[C:29]3=[O:30])[C:18]([O:20][CH2:21][CH3:22])=[O:19])[N:16]=2)[CH:6]=[CH:7][CH:8]=1

Participants

6

Procedure

Following a procedure similar to that described in Example 1, the desired compound was prepared from 1.75 g of ethyl 2-(3-m-methoxyphenylureido)thiazol-4-ylglyoxylate, 0.95 g of rhodanine-3-acetic acid, 0.5 g of ammonium chloride, 0.5 ml of 28% v/v aqueous ammonia and 20 ml of ethanol. The resulting product was a yellow powder having the following physical properties.

Sources & evidence

ORD record
ord-10ead3264fbc45379aafbd5bb7e37a22
Source dataset
uspto-grants-1990_06
Patent number
US04933355

Reaction notes

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