4-pyrrolidinopyridine

CCCCCCCCCCOc1ccc(-c2nc3cc(C(=O)OCCCCCCCC)ccc3o2)cc1
Reaction #5377
2-(4-decyloxyphenyl)-5-octyloxycarbonyl benzooxazole
Выход 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #5640
product
Выход 649.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
Reaction #50880
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C(C)(C)C)n[nH]3)c2)CN1C(=O)OC(C)(C)C
Reaction #73366
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CCCCCCCBr)OCc1ccccc1
Reaction #77178
Benzyl-8-bromoctanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOCc1nc2c(N3C(=O)c4ccccc4C3=O)nc3ccccc3c2n1CC(C)(C)OC(=O)CN1C(=O)c2ccccc2C1=O
Reaction #91971
product
Выход 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(Cl)nc2c1CN(C(=O)CC(=O)C1CC1)CC2
Reaction #168008
1-(2-chloro-4-methyl-7,8-dihydro-1,6-naphthyridin-6(5H)-yl)-3-cyclopropylpropane-1,3-dione
Выход 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CC(=O)Nc1cccc(Nc2nccc(Sc3ccccc3)n2)c1
Reaction #168899
desired product
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(C(=O)Nc2cccc(C(C)Nc3cncc(Cl)n3)c2)cn1
Reaction #179117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #182966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Cl)CC(C)Oc1ccc(-c2ccc(C(=O)Oc3ccc(C#N)cc3)cc2)cc1
Reaction #192837
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCc1ccc(C(=O)Oc2ccc(OCCC[Si](C)(C)CCCC)cc2)s1
Reaction #193894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #226164
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCCC(=O)Oc1cc(-n2c(OC)nc(C(F)(F)C(F)(F)F)c(F)c2=O)c(F)cc1Cl
Reaction #273447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CNC(=O)OC1Cc2ccc(N3CCN(C4COC4)CC3)cc2C1NC(=O)c1ccc(F)cc1
Reaction #281853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
Reaction #319610
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCCCCCCCCCc1ncc(-c2ccc(OC(=O)CCCCCC)cc2)s1
Reaction #321751
2-decyl-5-(4-heptanoyloxyphenyl)thiazole
Выход 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCCCCCc1ccc(-c2ncc(-c3ccc(OC(=O)CCCCC)cc3)s2)cc1
Reaction #321754
2-(4-hexylphenyl)-5-(4-hexanoyloxyphenyl)thiazole
Выход 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
NNc1cc(N2CCC(N3CCCC3)CC2)ncn1
Reaction #329433
4-Hydrazino-6-(4-pyrrolidin-1-ylpiperidin-1-yl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C(C)C(=O)[O-].OCCCc1ccncc1
Reaction #332313
4-pyridinepropanol methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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