子结构搜索

COCC(N)=S

CCOC(=O)C(=N)N(N)C=O
Reaction #11325
(N-formylhydrazino)-imino acetic acid ethyl ester
收率 76.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)c1nc([C@@H]2C[C@@H](OS(C)(=O)=O)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)cs1
Reaction #65549
(2S, 4R)-2-[2-(dimethoxymethyl)thiazol-4-yl]-4-methanesulfonyloxy-1- (4-nitrobenzyloxycarbonyl)pyrrolidine
收率 60.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(CCl)cs1
Reaction #71070
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(CCl)cs1
Reaction #82698
4-Chloromethyl-2-methoxymethyl-1,3-thiazole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCNC1=S
Reaction #158355
ethyl (3S)-2-thioxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylate
收率 142.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCN=C1SC
Reaction #158356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(Nc2ncc(F)c(Nc3ccc4c(c3)NC(=S)CO4)n2)c1
Reaction #158813
N4-[2H-1,4-benzoxazin-3(4H)-thione-6-yl]-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCNC2=COc3ccc(Nc4nc(Nc5cccc(O)c5)ncc4F)cc3N12
Reaction #158814
5-fluoro-N2-(3-hydroxyphenyl)-N4-[1-oxo-1,2,3,6-tetrahydropyrimido[2,1-c][1,4]benzoxazin-9-yl]-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
S=C1COCc2cc(Cl)ccc2N1
Reaction #159357
title compound
收率 107.5%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(Nc2ncc(F)c(Nc3ccc4c(c3)NC(=S)CO4)n2)c1
Reaction #163924
N4-[2H-1,4-benzoxazin-3(4H)-thione-6-yl]-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCNC2=COc3ccc(Nc4nc(Nc5cccc(O)c5)ncc4F)cc3N12
Reaction #163925
5-fluoro-N2-(3-hydroxyphenyl)-N4-[1-oxo-1,2,3,6-tetrahydropyrimido[2,1-c][1,4]benzoxazin-9-yl]-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(Br)c2)COCC(=S)N1
Reaction #168697
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(Br)c2)COCC(N)=N1
Reaction #168698
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FCC1(c2cccc(Br)c2)COCC(=S)N1
Reaction #168709
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=NC(c2cccc(Br)c2)C(CF)OC1
Reaction #168710
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)C1(c2cccc(Br)c2)COCC(=S)N1
Reaction #168721
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Br)cc1C1(C(F)F)COCC(=S)N1
Reaction #168726
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC(c2cc(Br)ccc2F)(C(F)F)COC1
Reaction #168727
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(c2cc(Br)ccc2[N+](=O)[O-])COCC(N)=N1
Reaction #168741
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(c2cccc(Br)c2)CO[C@@](C)(C(F)(F)F)C(N)=N1
Reaction #168748
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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