EtOAc

S=C(NCc1ccccc1)Nc1ccc(NC(=S)NCc2ccccc2)cc1
Reaction #852
colorless crystal
Выход 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(NC(=S)NC(=O)c2ccccc2)c(C)cc1NC(=S)NC(=O)c1ccccc1
Reaction #853
colorless crystal
Выход 98.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
S=C(NCc1ccccc1)Nc1cccc2c(NC(=S)NCc3ccccc3)cccc12
Reaction #854
colorless crystal
Выход 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(OCCC2OCCCO2)cc1
Reaction #879
4-(2-[1,3]-dioxane-2-yl-ethoxy)benzaldehyde
Выход 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(OCCC2OCCO2)cc1
Reaction #881
4-(2-[1,3]-dioxolan-2-yl-ethoxy)benzaldehyde
Выход 104.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC(O)CCCOC(=O)c1ccccc1
Reaction #884
4-hydroxy-nonyl benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1
Reaction #908
N-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccn(C)c1S(=O)(=O)NC(C)(C)C
Reaction #924
title compound
Выход 14.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)c2cccc(N)c2C#N)c1
Reaction #939
2-amino-6-[(3,5-dimethylphenyl)sulfinyl]benzonitrile
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)(=O)c2cccc(N)c2C#N)c1
Reaction #940
2-amino-6-[(3,5-dimethylphenyl)sulfonyl]benzonitrile
Выход 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
Reaction #986
171
Выход 102.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H]1COS(=O)(=O)N1c1ccccn1
Reaction #990
(R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine-2,2-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC#C[C@H](C)Oc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC
Reaction #1031
title compound
Выход 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CC(F)=C(F)F)n1cncn1
Reaction #1044
desired product
Выход 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1088
[3-(4-benzyloxy)phenoxy]benzo-[b]thiophene
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2cc(B(O)O)sc2c1
Reaction #1089
6-methoxybenzo[b]thiophene-2-boronic acid
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)NC(=S)CNc1ccc(C(=O)OC)c(S(=O)(=O)NC(C)(C)C)c1
Reaction #1095
N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamide
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CC(C)(O)Cc1cncc(C2CCCN2C(=O)OC(C)(C)C)c1
Reaction #1138
5-(2-hydroxy-2-methyl-3-butynyl)-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine
Выход 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1C(=O)CCC1c1cncc(Br)c1
Reaction #1140
5-bromo-3-(1-methyl-5-pyrrolidin-2-onyl)pyridine
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1cc2ccc(O)cc2o1
Reaction #1151
methyl 6-hydroxybenzofuran-2-carboxylate
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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