部分構造検索

CCN(CC)CCCl

Cl.O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2554
title compound
収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2555
title compound
収率 92.3%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2564
title compound
収率 54.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.ClCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3928
1-(4-chlorobenzyl)-4-(2-chloroethyl)piperazine dihydrochloride
収率 112.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.SCCN1CCN(Cc2ccc(Cl)cc2)CC1
Reaction #3929
2-[4-(4-chlorobenzyl)piperazin-1-yl]ethanethiol dihydrochloride
収率 97.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(OCCN(Cc2ccccc2)Cc2ccccc2)c1O
Reaction #4642
3-(2-dibenzylaminoethoxy)salicyclic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCl
Reaction #5368
N-(2-chloroethyl)-phthalimide
収率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CCN2CCOCC2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O.O=CO
Reaction #7420
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NOCCN1CCOCC1)c1ccccc1
Reaction #10272
acetophenone O-[2-((morpholin-4-yl))ethyl]oxime
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(OCCC2CNCCO2)c2ccsc2c1
Reaction #11523
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(=O)c1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11718
title compound
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)CCl
Reaction #11721
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11722
title compound
収率 94.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)CCl
Reaction #11727
title compound
収率 84.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11728
title compound
収率 92.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C=O
Reaction #11731
title compound
収率 84.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CN1C(=O)c2ccccc2C1=O
Reaction #11735
title compound
収率 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11748
title compound
収率 97.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(N)(=O)=O
Reaction #11759
title compound
収率 70.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CS(N)(=O)=O
Reaction #11766
title compound
収率 30.8%DOI: 10.6084/m9.figshare.5104873.v1
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