部分構造検索

1284323

O=C1N(C2CCC(O)CC2)CCC12CCNCC2
Reaction #182036
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2CCC3(CC2)CCN(C2CCC(O)CC2)C3=O)cc1
Reaction #211961
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)N1CCC2(CC1)CCN([C@H]1CC[C@H](O)CC1)C2=O
Reaction #303131
benzyl 2-(trans-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate
収率 72.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N([C@H]2CC[C@H](O)CC2)CCC12CCNCC2
Reaction #303132
2-(trans-4-hydroxycyclohexyl)-2,8-diazaspiro[4.5]decan-1-one
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2CCC3(CC2)CCN([C@H]2CC[C@H](O)CC2)C3=O)cc1
Reaction #303133
4-[2-(trans-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]dec-8-yl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC2(CC1)CCN([C@H]1CC[C@@H](O)CC1)C2=O
Reaction #303134
benzyl 2-(cis-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]decane-8-carboxylate
収率 72.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N([C@H]2CC[C@@H](O)CC2)CCC12CCNCC2
Reaction #303135
2-(cis-4-hydroxycyclohexyl)-2,8-diazaspiro[4.5]decan-1-one
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N([C@H]2CC[C@@H](O)CC2)CCC12CCN(c1ncccc1F)CC2
Reaction #303136
8-(3-fluoropyridin-2-yl)-2-(cis-4-hydroxycyclohexyl)-2,8-diazaspiro[4.5]decan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc([N+](=O)[O-])cnc1N1CCC2(CC1)CCN([C@H]1CC[C@@H](O)CC1)C2=O
Reaction #303137
2-(cis-4-Hydroxycyclohexyl)-8-(3-methyl-5-nitropyridin-2-yl)-2,8-diazaspiro[4.5]decan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)cnc1N1CCC2(CC1)CCN([C@H]1CC[C@@H](O)CC1)C2=O
Reaction #303138
8-(5-amino-3-methylpyridin-2-yl)-2-(cis-4-hydroxycyclohexyl)-2,8-diazaspiro[4.5]decan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Nc1cnc(N2CCC3(CC2)CCN([C@H]2CC[C@@H](O)CC2)C3=O)c(C)c1
Reaction #303139
methyl {6-[2-(cis-4-hydroxycyclohexyl)-1-oxo-2,8-diazaspiro[4.5]dec-8-yl]-5-methylpyridin-3-yl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCCC2=O)cnc1N1CCC2(CC1)CCN([C@H]1CC[C@@H](O)CC1)C2=O
Reaction #303140
2-(cis-4-hydroxycyclohexyl)-8-[3-methyl-5-(2-oxopyrrolidin-1-yl)pyridin-2-yl]-2,8-diazaspiro[4.5]decan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cccc(-c2cnc(N3CCC4(CC3)CCN([C@H]3CC[C@@H](O)CC3)C4=O)c(Cl)c2)c1
Reaction #303141
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N([C@H]2CC[C@@H](O)CC2)CCC12CCN(c1cc(Br)ccc1F)CC2
Reaction #303142
desired product
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2ccc(F)c(N3CCC4(CC3)CCN([C@H]3CC[C@@H](O)CC3)C4=O)c2)cn1)N1CCCC1
Reaction #303144
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2ccc(F)c(N3CCC4(CC3)CCN(C3CCC(O)CC3)C4=O)c2)cn1)N1CCCC1
Reaction #369646
DOI: 10.1039/C8SC04228D
Cc1cc(N)cnc1N1CCC2(CC1)CCN(C1CCC(O)CC1)C2=O
Reaction #768954
DOI: 10.1039/C8SC04228D
Cc1cc([N+](=O)[O-])cnc1N1CCC2(CC1)CCN(C1CCC(O)CC1)C2=O
Reaction #923473
DOI: 10.1039/C8SC04228D
Cc1cc(N2CCCC2=O)cnc1N1CCC2(CC1)CCN(C1CCC(O)CC1)C2=O
Reaction #1239045
DOI: 10.1039/C8SC04228D
COC(=O)Nc1cnc(N2CCC3(CC2)CCN(C2CCC(O)CC2)C3=O)c(C)c1
Reaction #2247668
DOI: 10.1039/C8SC04228D