EtOAc

CCOC(=O)CC1(OC(C)=O)CCC(C)(C)c2ccc(Br)cc21
Reaction #1495
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(C(=O)Oc3ccc(C(=O)OCc4ccccc4)cc3)ccc21
Reaction #1497
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CF
Reaction #1532
pure title compound
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CCl
Reaction #1535
pure title compound
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1c(C(F)(F)F)nc(-c2ccccc2)n(CC(C)=O)c1=O
Reaction #1550
5-ethyl-3-(2-oxopropyl)-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCn1c(-c2ccccc2)nc(C(F)(F)F)cc1=O
Reaction #1551
3-methoxymethyl-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCn1c(-c2cccc(C=O)c2)nc(CC)c(CC)c1=O
Reaction #1553
5,6-diethyl-2-(3-formylphenyl)-3-propargyl-4(3H)-pyrimidinone
Выход 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CN=CN(c2cc(N)c(F)cc2Cl)C1
Reaction #1562
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CNC(=O)Nc1ccc(F)c(N)c1
Reaction #1564
title product
Выход 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2cc(N)c(F)cc2Cl)c1=O
Reaction #1568
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1ccc(Cl)cc1F
Reaction #1573
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCNC(=O)Nc1cc(NC(C)=O)c(F)cc1Cl
Reaction #1576
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCn1c(=O)[nH]c(=O)n(-c2cc(N)c(F)cc2Cl)c1=O
Reaction #1578
title product
Выход 82.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCn1c(=O)[nH]c(=O)n(-c2cc(N3C(=O)C4=C(CCCC4)C3=O)c(F)cc2Cl)c1=O
Reaction #1579
title product
Выход 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C2=C(CCCC2)C(=O)N1c1ccc(Cl)cc1F
Reaction #1580
title product
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #1582
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1(C(=O)OCC)Oc2ccc(C[C@@H](C)N)cc2O1.Cl
Reaction #1621
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
Reaction #1647
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC1CCC(n2cc(C)c(=O)[nH]c2=O)O1
Reaction #1652
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(C=Cc1ccccc1)Nc1ccc(Cl)cc1
Reaction #1671
amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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