Substructure Search

ClCCl.N

CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1N=CC(C(Cl)Cl)=NC1=NO
Reaction #4538
colorless crystals
Yield 67.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4540
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N(C)C(=O)Nc1nc(C(Cl)(Cl)Cl)ns1
Reaction #56273
product
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)NC(=O)c1ccccc1)C(=O)Nc1nc(C(Cl)(Cl)Cl)ns1
Reaction #56275
residue
Yield 35.5%DOI: 10.6084/m9.figshare.5104873.v1
CO.ClC(Cl)Cl.O.[NH4+].[OH-]
Reaction #74293
CHCl3 MeOH NH4OH H2O
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2n(C)c3ccccc3n2c1C(=O)C(Cl)(Cl)Cl
Reaction #82977
2,9-Dimethyl-3-trichloroacetylimidazo[1,2-a]benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)Nc2nc(C(Cl)(Cl)Cl)ns2)c1
Reaction #95214
pure product
Yield 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2nc(C(Cl)(Cl)Cl)ns2)cc1
Reaction #95215
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1cccc([N+](=O)[O-])c1
Reaction #95217
pure product
Yield 69.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1ccc([N+](=O)[O-])cc1
Reaction #95218
pure product
Yield 73.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1
Reaction #95219
pure product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1ccccc1Cl
Reaction #95220
crude product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1ccccc1F
Reaction #95221
pure product
Yield 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1c(Cl)cccc1Cl
Reaction #95222
pure product
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc(C(Cl)(Cl)Cl)ns1)c1ccc(Cl)cc1Cl
Reaction #95223
pure product
Yield 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(COc3ccccc3)SC21)N1CCOCC1
Reaction #96108
2,2,2-trichloroethyl α-[3-phenoxymethyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(Cc3ccccc3)SC21)N1CCOCC1
Reaction #96110
2,2,2-trichloroethyl α-[3-benzyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1
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