4-(Chloromethyl)-1,3-thiazole → HCID 19434382, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([NH:10][C:11]2[CH:12]=[N:13][CH:14]=[N:15][CH:16]=2)=[N:8][CH:9]=1)([O-:3])=[O:2].Cl[CH2:18][C:19]1[N:20]=[CH:21][S:22][CH:23]=1>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:10]([C:11]2[CH:16]=[N:15][CH:14]=[N:13][CH:12]=2)[CH2:18][C:19]2[N:20]=[CH:21][S:22][CH:23]=2)=[N:8][CH:9]=1)([O-:3])=[O:2]Participants
3
Procedure
Starting compounds: 5-[N-(5-nitro-2-pyridyl) amino]pyrimidine and 4-chloromethylthiazole
Sources & evidence
- ORD record
- ord-ad35de948fcf4cffac459f9c02c48a8c
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05538976
Reaction notes
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