Pyrithiobac → HCID 18462483, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([C:11]([C:13]2[C:14]([C:19]([N:21](C)[CH3:22])=[O:20])=[N:15][CH:16]=[CH:17][CH:18]=2)=[O:12])[N:4]=1.ClC1C(C(C2N=C(OC)C=C(OC)N=2)=O)=C(C(Cl)=CC=1)C(O)=O.ClC1C(C(O)=O)=C(SC2N=C(OC)C=C(OC)N=2)C=CC=1>>[CH3:10][O:9][C:7]1[CH:8]=[C:3]([O:2][CH3:1])[N:4]=[C:5]([CH:11]([OH:12])[C:13]2[C:14]([C:19]([NH:21][CH3:22])=[O:20])=[N:15][CH:16]=[CH:17][CH:18]=2)[N:6]=1Participants
4
Procedure
4, 7-dichloro-3-(4,6-dimethoxy-2-pyrimidnyl)-3-hexanoyloxyphthalide; 3-[(4,6-dimethoxy-2-pyrimidinyl)carbonyl]-N,N-dimethyl-2-pyridine carboxamide; 3,6-dichloro-2-[(4, 6-dimethoxy-2-pyrimidinyl)carbonyl]benzoic acid; 6-chloro-2-[(4,6-dimethoxy-2-pyrimidinyl)thio]benzoic acid (a.k.a. DPX-PE350 or pyrithiobac) and salts thereof.
Sources & evidence
- ORD record
- ord-9d9506eea9da4d969ec24fba8756747b
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05716901
Reaction notes
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