1-Naphthaldehyde → HCID 58981050, compound

HRID 1181753Notes

Reaction equation

HRID 1181753 reaction equation
[NH:1]([C:3]1[N:8]([CH2:9][CH:10]([CH3:12])[CH3:11])[C:7](=[O:13])[N:6]([CH3:14])[C:5](=[O:15])[CH:4]=1)[NH2:2].[C:16]1([CH:26]=O)[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH:19]=[CH:18][CH:17]=1.[CH3:28][C:29]1[CH:33]=[CH:32][S:31][C:30]=1[CH:34]=O>>[CH2:9]([N:8]1[C:3]2=[N:1][N:2]([CH2:26][C:16]3[C:25]4[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=4)[CH:19]=[CH:18][CH:17]=3)[C:34]([C:30]3[S:31][CH:32]=[CH:33][C:29]=3[CH3:28])=[C:4]2[C:5](=[O:15])[N:6]([CH3:14])[C:7]1=[O:13])[CH:10]([CH3:11])[CH3:12]

Participants

4

Procedure

This compound was made following the procedure described above, starting with 6-hydrazino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione, and condensing first with 1-naphthaldehyde, followed by 3-methylthiophene-2-carbaldehyde. Mass: 458.87 (M+H).

Sources & evidence

ORD record
ord-7b08aef2b21d4f5aa569e6cbf175b6f2
Source dataset
uspto-grants-2007_10
Patent number
US07285558B2

Reaction notes

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