子结构搜索

111682

Br.Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #77234
(R)-N-[5-methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphtyl]-4-morpholinobenzamide monohydrobromide
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CCC(NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #196297
DOI: 10.1039/C8SC04228D
Cc1ccc(N2CCN(C)CC2)c2c1CCC(NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #374775
DOI: 10.1039/C8SC04228D
CCc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #514527
title compound
收率 118.5%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #514530
title compound
收率 152.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #514531
title compound
收率 146.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=S(=O)(O)c1ccccc1
Reaction #514533
(R)-N-[5-Methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide Benzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=S(=O)(O)CCS(=O)(=O)O
Reaction #514534
(R)-N-[5-Methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide Hydrogen 1,2-Ethanedisulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=C(O)/C=C\C(=O)O
Reaction #514535
(R)-N-[5-Methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide Hydrogen Maleate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=C(O)CCC(=O)O
Reaction #514536
white solid
收率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O.Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #514537
(R)-N-[5-Methyl-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-4-morpholinobenzamide Methansulfonate
收率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=C(O)C[C@H](O)C(=O)O
Reaction #514538
white crystals
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #514539
white crystals
收率 62.4%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccc(N2CCN(C)CC2)c2c1CCC(NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #889849
DOI: 10.1039/C8SC04228D
CS(=O)(=O)O
Reaction #1203222
DOI: 10.1039/C8SC04228D
O=C(O)c1ccccc1O
Reaction #1317882
DOI: 10.1039/C8SC04228D
CCc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #1362094
title compound
收率 118.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #1362096
title compound
收率 146.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #1362111
title compound
收率 118.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCN(C)CC2)c2c1CC[C@@H](NC(=O)c1ccc(N3CCOCC3)cc1)C2
Reaction #1362113
title compound
收率 146.9%DOI: 10.6084/m9.figshare.5104873.v1
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