子结构搜索

1022

CCOC(=O)C1CCN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)CC1
Reaction #45706
oil
收率 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(N4CC[C@H](N(C)C)C4)c3o2)CC1
Reaction #45707
Ethyl 1-{4-cyano-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazol-2-yl}piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)ccc2cc1OCC(O)CN1CCC(C(O)(c2ccc(F)cc2)c2ccc(F)cc2)CC1
Reaction #50601
(±)-6-{3-[4-(bis(4-fluorophenyl)hydroxymethyl)-1-piperidinyl]-2-hydroxypropoxy}-7-methoxy-2H-1-benzopyran-2-one
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCC(C(O)(c2ccc(F)cc2)c2ccc(F)cc2)CC1)CCC3
Reaction #50633
8-{3-[4-(bis(4-fluorophenyl)hydroxymethyl)-1-piperidinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/C(=O)O.O=C(c1cnc(OC2CN3CCC2CC3)nc1C(F)(F)F)N1CCS(=O)(=O)CC1
Reaction #67074
3-({5-[(1,1-dioxidothiomorpholin-4-yl)carbonyl]-4-(trifluoromethyl)pyrimidin-2-yl}oxy)quinuclidine fumarate
收率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1CCN(Cc2ccccc2)CC1.[Na+]
Reaction #70570
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #73392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C[C@H](N)c2ccccc2)CC1
Reaction #92691
ethyl 1-[(2R)-2-amino-2-phenylethyl]piperidine-4-carboxylate
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[N+]12CCC(CC1)[C@@H](OC(=O)C(Nc1ccccc1)c1ccccc1)C2)c1ccc(F)cc1F.[Br-]
Reaction #164215
title compound
收率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)C[N+]23CCC(CC2)[C@@H](OC(=O)[C@H](Nc2ccccc2)c2ccccc2)C3)cs1.[Br-]
Reaction #164221
title compound
收率 35.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCN1CCC(C(O)(c2ccc(F)cc2)c2ccc(F)cc2)CC1)Nc1ccccc1
Reaction #174867
DOI: 10.1039/C8SC04228D
CC(=O)O
Reaction #176934
DOI: 10.1039/C8SC04228D
OCC1(Cc2ccccc2)CCNCC1
Reaction #178819
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #180950
DOI: 10.1039/C8SC04228D
CC1(C(=O)O)CCN(c2ccc(C(C)(C)C)cc2)CC1
Reaction #184506
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #186169
DOI: 10.1039/C8SC04228D
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #187616
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OCCCN2CCC(C(O)(c3ccc(F)cc3)c3ccc(F)cc3)CC2)c(OC)c1
Reaction #188489
DOI: 10.1039/C8SC04228D
COc1ccc2[nH]cc(C(=O)OCC34CCN(CC3)CC4)c2c1
Reaction #191517
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #192776
DOI: 10.1039/C8SC04228D
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