HCID 12256280, compound → HCID 21394538, compound

HRID 460761Notes

Reaction equation

HRID 460761 reaction equation
[CH2:1]([N:3]1[C:7]2[N:8]=[CH:9][C:10]3[C:15](=[O:16])[N:14]4[N:17]=[C:18]([C:20]5[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=5)[CH:19]=[C:13]4[NH:12][C:11]=3[C:6]=2[CH:5]=[N:4]1)[CH3:2].[CH3:26][S:27][CH2:28]Br>>[CH2:1]([N:3]1[C:7]2[N:8]=[CH:9][C:10]3[C:15](=[O:16])[N:14]4[N:17]=[C:18]([C:20]5[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=5)[CH:19]=[C:13]4[N:12]([CH2:26][S:27][CH3:28])[C:11]=3[C:6]=2[CH:5]=[N:4]1)[CH3:2]

Participants

3

Reactant 2

HCID 12256280HCID 12256280, compoundHCID 178462994HCID 178462994, compound

Product 1

HCID 21394538HCID 21394538, compound

Procedure

By treating the product of Example 29 with methylthiomethyl bromide according to the procedure of Example 2, 3-ethyl-3,11-dihydro-9-phenyl-11-methylthiomethyl-6H-pyrazolo[1,5-a]pyrazolo[4',3':5,6]pyrido[4,3-d]pyrimidin-6-one is obtained.

Sources & evidence

ORD record
ord-f3c31c5a5b7e4a9abfdc979b98d1d038
Source dataset
uspto-grants-1977_12
Patent number
US04061632

Reaction notes

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