N-methylpyrrolidine

CCc1ccc(N2CCC(CO)CC2)nn1
Reaction #5038
Formula IV
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc2cnn(-c3ccc(F)cc3)c2cc1Cl
Reaction #41398
1-(4-Fluorophenyl)-6-chloro-5-methoxy-1H-indazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(-c4nc(N)c(F)cc4F)c3c2Br)C1
Reaction #53453
title compound
수율 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)C(=NOC(F)F)c3csc(NC(c4ccccc4)(c4ccccc4)c4ccccc4)n3)[C@H]2S(=O)C1)[NH+]1CCCC1.[I-]
Reaction #62780
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(1-methyl-1-pyrrolidiniomethyl)-3-cephem-4-carboxylate-1-oxide iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Nc1ccc(-c2cc3nc(Cl)nc(N4CCOCC4)c3s2)cn1
Reaction #70164
2-chloro-6-(6-aminopyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1ccnc2[nH]c3cnccc3c12
Reaction #88536
4-Chloro-9H-dipyrido[2,3-b;4′,3′-d]pyrrole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1nc(-n2cc(C(=O)O)c(=O)c3cc(F)c(N4CC(N)C4)c(Br)c32)ccc1F
Reaction #177552
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1nccs1)NC(Cc1ccccc1)(c1ccc(F)cc1)c1cc(F)cc(OC(F)(F)C(F)F)c1
Reaction #181850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1cccc(N)c1C
Reaction #187534
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)OC(=O)NC1Cc2c(n(CC3OCCC3O)c3ccc(C#N)cc23)C1
Reaction #190599
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C1c2nc[nH]c2CCN1C(=O)OCC1CCCN1C
Reaction #204325
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(-c4nc(N)c(F)cc4C)c3c2Cl)C1
Reaction #207912
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)n2cc(C(F)(F)F)c3c(Cl)ccnc32)cc1
Reaction #221240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCC(c1cc(C#N)cs1)n1ccnc1
Reaction #227872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC[N+]1(C)CCCC1
Reaction #230671
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nc(-n2cc(C(=O)O)c(=O)c3cc(F)c(N4CC(N)C4)c(F)c32)c(F)cc1F
Reaction #231262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nc(=O)n(C2CC(CO)C2)cc1F
Reaction #232611
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C1CC(Oc2cc(-c3ccccc3)nc3cc(OC)c(Br)cc23)CN1C(=O)OC(C)(C)C
Reaction #256308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CNC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(-c4nc(N)c(F)cc4F)c3c2F)C1
Reaction #258868
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)C#Cc1ncc(C#N)cn1
Reaction #265125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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