子结构搜索

107697

CCCN(CCC)C1COc2c(F)ccc(-c3ccco3)c2C1
Reaction #65946
3-dipropylamino-8-fluoro-5-(2-furyl)chroman
收率 52.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65947
title compound
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(CC)CC)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65954
(R)-8-fluoro-5-methyloxycarbonyl-3-(N-3-pentyl-N-n-propylamino)chroman
DOI: 10.6084/m9.figshare.5104873.v1
N
Reaction #65955
NH3
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #65956
title compound
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80543
title compound
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN([C@H]1COc2c(F)ccc(C(=O)OC)c2C1)C(C)(C)C
Reaction #80547
Methyl (R)-3-(N-tert-Butyl-N-n-propylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(F)c2c1C[C@@H](N(C1CCC1)C1CCC1)CO2
Reaction #80549
title compound
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C1CCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80552
title compound
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(F)c2c1C[C@@H](N(C(C)C)C1CCC1)CO2
Reaction #80556
title compound
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C1CCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80559
title compound
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C1CCCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80562
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(F)c2c1C[C@@H](N(C1CCCC1)C1CCC1)CO2
Reaction #80566
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)N
Reaction #156514
designed compound
收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1C[C@H](C)N=[N+]=[N-]
Reaction #156521
(S)-2-(2-azidopropyl)-4-fluoro-1-methylbenzene
收率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C(C)C)C3=O
Reaction #156551
title compound
收率 127.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)CN(C(C)C)C3=O
Reaction #156553
2-(4-((1-(5-Fluoro-2-methylphenyl) propan-2-yl)amino)-2-oxo-1,2-dihydropyridin-3-yl)-6-isopropyl-6,7-dihydroimidazo[4,5-f]isoindol-5(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)CN(C)C3=O
Reaction #156564
2-(4-(1-(5-Fluoro-2-methylphenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methyl-6,7-dihydroimidazo[4,5-f]isoindol-5(1H)-one
收率 82.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(CCN(C)C)C3=O
Reaction #156565
2-(4-(1-(5-Fluoro-2-methylphenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-(2-(dimethylamino)ethyl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione
收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)cc1CC(C)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)CN(CCN(C)C)C3=O
Reaction #156566
2-(4-(1-(5-Fluoro-2-methylphenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-(2-(dimethylamino)ethyl)-6,7-dihydroimidazo[4,5-f]isoindole-5(1H)-one
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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