部分構造検索

C(CF)N

C[C@H](NC(=O)C(F)F)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41326
2,2-Difluoro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CF)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41327
2-Fluoro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)CF)c1
Reaction #41333
2-Fluoro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCN(CCF)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #60704
title compound
収率 32.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1(N2CCN(C3CC3)CC2)CCNCC1)C(F)(F)F
Reaction #74274
desired product
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82736
title compound
収率 55.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82739
title compound
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCn2c(nnc2C(F)(F)F)C1
Reaction #90752
ethyl 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine-7-carboxylate
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc([N+](=O)[O-])c(N3CCCC(F)C3)c2)CC1
Reaction #173604
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)N2CC(F)(F)OC3(CCN(Cc4cccc(CCO)c4)CC3)C2)s1
Reaction #186572
DOI: 10.1039/C8SC04228D
CC1(c2cc(NC(=O)c3cnc(C(F)(F)F)cn3)ccc2F)N=C(N)OCC1(F)F
Reaction #188959
DOI: 10.1039/C8SC04228D
O=C(NC(c1ccccn1)C(F)(F)F)c1ccc(N2CC(F)(F)C2)c(OCC2CC2)n1
Reaction #193310
DOI: 10.1039/C8SC04228D
CC1(c2cc(NC(=O)c3ccc(OCC(F)(F)C(F)(F)F)cn3)ccc2F)N=C(N)OCC1(F)F
Reaction #193456
DOI: 10.1039/C8SC04228D
Nc1nc(OCc2ccc(CNC(=O)C(F)(F)F)cc2)c2nc[nH]c2n1
Reaction #193745
DOI: 10.1039/C8SC04228D
CCn1cc(Cl)c(C(=O)Nc2ccc(F)c(C3(C)N=C(N)OCC3(F)F)c2)n1
Reaction #200288
DOI: 10.1039/C8SC04228D
O=C1Nc2ccc([N+](=O)[O-])cc2C(c2ccccc2)=NC1F
Reaction #203662
DOI: 10.1039/C8SC04228D
O=C(NC(COCC1CCN(CCF)CC1)c1ccccc1Cl)c1ccc2c(Cl)c[nH]c2c1
Reaction #211690
DOI: 10.1039/C8SC04228D
CC(C)N1CCOC(COc2ccc3c(c2)cc(C(=O)N2CCOCC2)n3CC(F)(F)F)C1
Reaction #219997
desired product
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cc(NC(=O)c3[nH]nc(C4CC4)c3Cl)ccc2F)N=C(N)OCC1(F)F
Reaction #221297
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1ccc(Oc2ccnc3cc(OC)c(C(=O)NC4CC4F)cc23)cc1F
Reaction #226929
DOI: 10.1039/C8SC04228D
1 ページ次のページ