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CN1CCCC1CCN

CN1CCCC1CCN=C=S
Reaction #7907
2-(2-isothiocyanatoethyl)-1-methylpyrrolidine
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC1CCNC(N)=S
Reaction #7908
[2-(1-methylpyrrolidin-2-yl)ethyl]thiourea
DOI: 10.6084/m9.figshare.5104873.v1
C(=NC1CCN2CCCC2C1)c1ccncc1
Reaction #9969
title compound
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ncn(C3CCN4CCCC4C3)c2-c2ccncc2)cc1
Reaction #9970
title compound
Ausbeute 14.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49235
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N3CCC[C@@H]3COC)c2)C1
Reaction #49239
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC4CC3C(=O)N4Cc3cc4c(cn3)OCCO4)c2c1
Reaction #68284
1-(2-(6-(2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)-7-oxo-2,6-diazabicyclo(3.2.1)oct-2-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC1CCN=C=S
Reaction #75551
2-(2-isothiocyanatoethyl)-1-methylpyrrolidine
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC1CCNC(N)=S
Reaction #75552
[2-(1-methylpyrrolidin-2-yl)ethyl]thiourea
DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c(C=O)c(C)c1C(=O)NCCC1CCCN1C
Reaction #160429
N-[(1-methylpyrrolidin-2-yl)ethyl]-5-formyl-2,4-dimethyl-1H-pyrrole-3-formamide
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccc3c(c2)OCO3)CCN(C(=O)c2ccc(Cl)c(S(N)(=O)=O)c2)CC1
Reaction #177962
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(C(=O)N1CCC2C1C(c1c[nH]c3cc(F)ccc13)CN2C(=O)Cc1ccccc1)C1CCCCC1
Reaction #181862
DOI: 10.1039/C8SC04228D
c1ccc(CN2CCCC23CCN(c2cccnc2)C3)cc1
Reaction #189669
DOI: 10.1039/C8SC04228D
CCC(N)C(=O)N1CCC2C1C(c1c[nH]c3cc(F)ccc13)CN2S(C)(=O)=O
Reaction #190623
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccccc2)CCN(C(=O)c2cc(Cl)ccc2S(=O)(=O)NC2CC2)CC1
Reaction #191993
DOI: 10.1039/C8SC04228D
CN1CCCC1CCn1ccc2cc(CN)ccc21
Reaction #196205
DOI: 10.1039/C8SC04228D
CN1C2CCC1CC(N1CCN(C(=O)C(CC(=O)N3CCC(N4CCc5ccccc5NC4=O)CC3)Cc3cc(Cl)c(N)c(C(F)(F)F)c3)CC1)C2
Reaction #196832
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccccc2)CCN(C(=O)c2cc(Cl)ccc2S(=O)(=O)NC(C)C)CC1
Reaction #197815
DOI: 10.1039/C8SC04228D
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