Isocil → Bromacil

HRID 3624Notes

Reaction equation

[Br:1][C:2]1[C:3](=[O:17])[N:4]([CH:11]2[CH2:16]CC[CH2:13][CH2:12]2)[C:5](=[O:10])[N:6](C)[C:7]=1[CH3:8].C1CCC(N2C(=O)NC3CCCC=3C2=O)CC1.BrC1C(=O)N(C(C)C)C(=O)NC=1C.C(N1C(=O)C(Cl)=C(C)NC1=O)(C)(C)C>>[Br:1][C:2]1[C:3](=[O:17])[N:4]([CH:11]([CH2:12][CH3:13])[CH3:16])[C:5](=[O:10])[NH:6][C:7]=1[CH3:8]

Participants

Reactant 4

HCID 9412Isocil

HCID 16559Lenacil

HCID 22188Terbacil

HCID 232975055-Bromo-3-cyclohexyl-1,6-dimethyluracil

Product 1

HCID 9411Bromacil

Procedure

5-bromo-3-cyclohexyl-1,6-dimethyluracil; 3-cyclohexyl-5,6-trimethyleneuracil; 5-bromo-3-isopropyl-6-methyluracil; 3-tert-butyl-5-chloro-6-methyluracil;

Sources & evidence

ORD record: ord-1f5da75e69d34567ab43993557d098c2
Source dataset: uspto-grants-1998_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05733849

Reaction notes

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