参与 250 个反应

7727

CC(=O)Cc1nc2ccccc2s1
Reaction #4798
2-acetonylbenzothiazole
收率 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccc(N2CCOCC2)c2sc(NC(=O)c3ccnc(C)c3)nc12
Reaction #8444
N-(4-Methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-2-methyl-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1nc2ccccc2s1
Reaction #9668
2-amino-1,3-benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(=O)Nc1nc2ccccc2s1
Reaction #54746
desired product
收率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1nc2ccccc2s1
Reaction #59165
2-amino-1,3-benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)Nc1nc2ccccc2s1
Reaction #80835
title compound
收率 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
c1ccc(Nc2cn3c(n2)sc2ccccc23)cc1
Reaction #158202
(imidazo[2,1-b]benzothiazol-2-yl)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)C(C(=O)Nc2nc3ccccc3s2)C1(C)C
Reaction #165589
title compound
收率 27.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.COCCCn1c(=N)sc2ccccc21
Reaction #165590
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Br.COCCn1c(=N)sc2ccccc21
Reaction #165591
title compound
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1nc2ccccc2s1)C(=NOC1CCCC1)c1ccc(Cl)c(Cl)c1
Reaction #176741
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1OC(NC(=S)Nc2nc3ccccc3s2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #192919
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCC(=O)Nc1nc2ccccc2s1
Reaction #198616
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1C(C(=O)Nc2nc3ccccc3s2)=C(O)c2sc3ccccc3c2S1(=O)=O
Reaction #215444
N-(2-Benzothiazolyl)-4-hydroxy-2-methyl-2H-[1]benzothieno-[2,3-e]-1,2-thiazine-3-carboxamide-1,1-dioxide
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC(C)N(CCC(c1ccccc1)c1ccccc1)C(=O)Nc1nc2ccccc2s1
Reaction #221509
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NNC(=O)Nc1nc2ccccc2s1
Reaction #240766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1C(=O)Nc1nc2ccccc2s1
Reaction #255771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1ccccc1NC(=S)Nc1nc2ccccc2s1
Reaction #257893
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)c1ccc(C(CC2CCCC2)C(=O)Nc2nc3ccccc3s2)cc1[N+](=O)[O-]
Reaction #261436
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)ON=C(C(=O)Nc1nc2ccccc2s1)c1ccc(S(C)(=O)=O)c(Cl)c1
Reaction #273677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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