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CC(C)C(=O)Cl

CCCC(Cc1ccccc1Br)C(=O)Cl
Reaction #1355
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1ncnc2c1ncn2[C@H]1CC=CO1
Reaction #1654
(R)-N-[9-(2,3-Dihydro-2-furanyl)-9H-purin-6-yl]-2,2-dimethylpropanamide
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)C3CCCCC3)CC2)cc1
Reaction #1751
trans-O-cyclohexanoyl-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(NC(=O)C(C)(C)C)cn2)cc1
Reaction #2379
N-[6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl]pivalamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(NC(=O)C(C)(C)C)cc1
Reaction #2599
title compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNc1nc2cc(OC(=O)C(C)(C)C)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3253
title compound
Выход 83.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Oc1ccc(CCNC(=O)OCc2ccccc2)cc1OC(=O)C(C)(C)C
Reaction #6000
desired compound
Выход 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCCCSc1ccncc1.Cl
Reaction #6196
desired compound
Выход 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCCCOc1ccncc1
Reaction #6237
desired compound
Выход 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1cccc(C(F)(F)F)c1
Reaction #6521
solid
Выход 98.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1cc2c(O)nc[nH]c-2n1
Reaction #6620
4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
Выход 89.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC1C)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7647
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]-2-methylcyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC2C=CC1C2)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7650
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]bicyclo[2.2.1]hept-5-ene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C(C)(C)C)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7657
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(OC(=O)C(C)(C)C)CN1C(=O)OCc1ccccc1
Reaction #7751
desired product
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1cccnc1
Reaction #7872
N-(pyridin-3-yl)-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1c(C(=O)c2cccnc2)oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #8885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc(C)c(C)c2n1CCC1CCN(C(=O)[C@@H]2C[C@H]2c2ccccc2)CC1
Reaction #11468
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N)c2nc(C)n(CCCNC(=O)[C@@H]3C[C@H]3c3ccccc3)c2c1C
Reaction #11469
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(=O)(=O)NC(=O)C(C)(C)C
Reaction #11761
title compound
Выход 49.2%DOI: 10.6084/m9.figshare.5104873.v1
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