pyrrolidin-3-ol

OC1CCN(c2ccncc2)C1
Reaction #651
収率 43.0%750 AstraZeneca ELN dataset
OC1CCN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7543
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-pyrrolidinol
収率 54.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cn1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1N1CCC(O)C1
Reaction #41119
5-(3-Hydroxy-pyrrolidin-1-yl)-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)n1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1N1CCC(O)C1
Reaction #41137
1-tert-butyl-5-(3-hydroxy-pyrrolidin-1-yl)-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OC1CCN(c2cnc3nnn(Cc4ccc5ncccc5c4)c3n2)C1
Reaction #44285
1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-ol
収率 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN1c2ncccc2C(=O)Nc2c(C)cc(N3CCC(O)C3)nc21
Reaction #81821
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
OB(O)c1ccc(N2CCC(O)C2)nc1
Reaction #85826
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCC(O)C2)cn1
Reaction #170521
title compound
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OC1CCN(c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C1
Reaction #177220
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCN(c2ccccc2C(F)(F)F)C1
Reaction #181235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Nc1cc(F)cc(F)c1)c1cc(C(=O)N2CCC(O)C2)cc2c(=O)cc(N3CCOCC3)oc12
Reaction #182026
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cc(CN2CCC(O)C2)cc(C(F)(F)F)c1
Reaction #184648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCN(CC1CC1)c1cc(C(=O)Nc2ccc(CN3CCC(O)C3)cc2C)ncn1
Reaction #187146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)N1CCC(O)C1
Reaction #188073
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OC1CCNC1)c1ccccc1
Reaction #190668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC1CCN(c2cccc(Br)n2)C1
Reaction #195430
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1cnn2ccc(N3CCCC3c3cncc(F)c3)nc12)N1CCC(O)C1
Reaction #199877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1cc(Oc2cc(F)c(NC(=O)C3(C(=O)OCc4ccccc4)CC3)cc2F)ccn1)N1CCC(O)C1
Reaction #200443
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)c1ccc(CCN2CCC(O)C2)cc1
Reaction #201155
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(OC2CCNC2)cn1
Reaction #205758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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