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OC1(c2ccccc2)CCNCC1

Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(OCCO)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78349
expected product
Ausbeute 128.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78350
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCN1CCC(O)(c2ccccc2)CC1.Cl
Reaction #94242
4-(4-hydroxy-4-phenypiperidino)-2-butanone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)CC=C1c1ccc(C(F)(F)F)c2ccoc12
Reaction #174143
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(C(=O)NC(CC(=O)N2CCC(O)(c3ccc(Cl)cc3)C(C)(C)C2)C(C)C)c1
Reaction #177093
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)C1CCC(=O)C1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)C(C)(C)C1
Reaction #180421
DOI: 10.1039/C8SC04228D
CNC(=O)N1CCC(Oc2ccc(C(F)(F)F)cc2)(c2ccccc2)CC1
Reaction #180734
DOI: 10.1039/C8SC04228D
CC1(C)CN(C(=O)CC2(N)CCOCC2)CCC1(O)c1ccc(Cl)cc1
Reaction #183360
DOI: 10.1039/C8SC04228D
COc1cc(OC)c2c(C)c(CCN3CCC(O)(c4ccccc4)CC3)c(=O)oc2c1
Reaction #203934
DOI: 10.1039/C8SC04228D
OC1(c2ccc3ccccc3c2)CC2CCC(C1)N2
Reaction #217578
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)C(=O)C(CN1CCC(O)(c3ccccc3)CC1)CC2
Reaction #221903
DOI: 10.1039/C8SC04228D
Cl
Reaction #222323
DOI: 10.1039/C8SC04228D
OC1(c2ccc3cc(OCc4ccccc4)ccc3c2)CCN(CCCOc2cccc3[nH]ccc23)CC1
Reaction #222760
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(C(=O)c3cn(C(=O)c4cccc(F)c4F)c4cc(Cl)ccc34)CC2)c2ccc(Br)cc21
Reaction #224725
DOI: 10.1039/C8SC04228D
CCCOc1ccc2cc(C3(O)CCN(CC(O)COc4cccc5[nH]ccc45)CC3)ccc2c1
Reaction #236822
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(C(=O)c3cn(-c4cccc(-c5ccccc5)c4)c4cc(Cl)ccc34)CC2)c2ccccc21
Reaction #239180
DOI: 10.1039/C8SC04228D
Cc1cccc(C2(O)CCN(Cc3cncn3Cc3ccc(C#N)cc3)CC2)c1
Reaction #239399
DOI: 10.1039/C8SC04228D
O=CN1CCC(Oc2c(F)c(F)c(F)c(F)c2F)(c2ccccc2)CC1
Reaction #240136
DOI: 10.1039/C8SC04228D
Cl
Reaction #248741
DOI: 10.1039/C8SC04228D
Cl
Reaction #249277
DOI: 10.1039/C8SC04228D
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