urea

O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1606
5-(4-chlorophenyl)-2-pyrimidinone
المردود 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1674
5-(4-chlorophenyl)-2-pyrimidinone
المردود 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)c1ccc(-c2[nH]c(=O)[nH]c2-c2ccccc2)cc1
Reaction #1761
4-(4-dimethylaminophenyl)-2,3-dihydro-5-phenyl-1H-imidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2179
5-(4-chlorophenyl)-2-pyrimidinone
المردود 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2220
5-(4-chlorophenyl)-2-pyrimidinone
المردود 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)c1ccc(-c2[nH]c(=O)[nH]c2-c2ccccc2)cc1
Reaction #2231
4-(4-dimethylaminophenyl)-2,3-dihydro-5-phenyl-1H-imidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #2278
5-(4-chlorophenyl)-2-pyrimidinone
المردود 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C.NC(N)=O
Reaction #2764
Urea neopentane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)c1ccc(-c2[nH]c(=O)[nH]c2-c2ccccc2)cc1
Reaction #2819
4-(4-dimethylaminophenyl)-2,3dihydro-5-phenyl-1H-imidazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(N)=O.O=S(=O)(O)O
Reaction #3148
Urea Sulfuric Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCc1ccccc1
Reaction #4000
Normal-butylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Oc1nc(O)c2cnn(CCc3ccccc3)c2n1
Reaction #8397
title compound
المردود 105.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(O)cccc1C(=O)O
Reaction #8936
yellow solid
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(C23CC2C(=O)NC3=O)cc1
Reaction #10481
(±)-1-(4-methylphenyl)-3-azabicyclo[3.1.0]hexan-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCCC(=O)[C@H]1N(C(=O)[C@@H](O)[C@H](Cc2ccccc2)NC(=O)c2cccc(O)c2C)CSC1(C)C
Reaction #11268
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1coc(N)n1
Reaction #42612
ethyl 2-amino-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CCC(=O)NC1=O
Reaction #42857
3,3-dimethylpiperidin-2,6-dione
المردود 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CC(C)(C)C(=O)NC1=O
Reaction #42858
3,3,5,5-tetramethylpiperidin-2,6-dione
المردود 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)CC(=O)NC1=O
Reaction #42859
3,3-dimethylpyrrolidin-2,5-dione
المردود 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nc(-c2ccc(Oc3ccc(OC)cc3)cc2)cn1-c1ccc2c(c1)CNCC2.Cl
Reaction #46019
7-{2-butyl-4-[4-(4-methoxy-phenoxy)-phenyl]-imidazol-1-yl}-1,2,3,4-tetrahydro-isoquinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
الصفحة 1التالي