部分構造検索

17214

Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4127
product
収率 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4132
product
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4133
product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4185
product
収率 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4190
product
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4191
product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #61990
ammonia DCM
収率 1.0%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #61991
ammonia DCM
収率 1.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #62656
product
収率 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #62661
product
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #62662
product
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #63414
product
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OCc1cc(Oc2ccc3c(c2)CCN3C(=O)Nc2cccc(C(F)(F)F)c2)ncn1
Reaction #73382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(Cl)c1)N1CCc2ccccc21
Reaction #161689
(2-chloropyridin-4-yl)-(2,3-dihydroindol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(Cl)c1)N1CCc2cc(F)ccc21
Reaction #161690
(2-chloropyridin-4-yl)-(5-fluoro-2,3-dihydroindol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ccn1)N1CCc2cc(F)ccc21
Reaction #161691
(4-chloropyridin-2-yl)-(5-fluoro-2,3-dihydroindol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ccn1)N1CCc2c1ccc(F)c2F
Reaction #161730
(4-chloro-pyridin-2-yl)-(4,5-difluoro-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(Cl)c1)N1CCc2c1ccc(F)c2F
Reaction #161731
(2-chloro-pyridin-4-yl)-(4,5-difluoro-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccnc(Cl)c1)N1CCc2cc(F)c(F)cc21
Reaction #161762
(2-chloro-pyridin-4-yl)-(5,6-difluoro-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cncc(Br)c1)N1CCc2cc(F)ccc21
Reaction #161773
(5-bromo-pyridin-3-yl)-(5-fluoro-2,3-dihydro-indol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
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