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Brc1cccs1

OCCCc1sc(C2OCCO2)cc1Br
Reaction #43644
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C#Cc2ccc(S(=O)(=O)N[C@H](Cc3c[nH]c4ccccc34)C(=O)O)s2)cc1
Reaction #68771
(R)-3-(1H-Indol-3-yl)-2-(5-p-tolylethynyl-thiophene-2-sulfonylamino)-propionic acid
Ausbeute 55.4%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(S(=O)(=O)N[C@H](Cc2c[nH]c3ccccc23)C(=O)O)s1
Reaction #68772
(R)-3-(1H-Indol-3-yl)-2-(5-trimethylsilanylethynyl-thiophene-2-sulfonylamino)-propionic acid
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)c1ccc(Br)s1
Reaction #80458
2-bromo-5-(4-fluorophenylcarbonyl)thiophene
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCOC2CCCCO2)c(=O)c2c(CBr)c(Br)sc21
Reaction #92162
6-bromo-5-(bromomethyl)-1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Ausbeute 56.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)sc2c1c(=O)n(CCCO)c(=O)n2C
Reaction #92174
6-bromo-3-(3-hydroxypropyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Ausbeute 116.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(Cl)c(Cl)c2)sc2c1c(=O)n(CCCO)c(=O)n2C
Reaction #92175
6-(3,4-dichlorophenyl)-3-(3-hydroxypropyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Ausbeute 27.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCn1c(=O)c2c(C)c(-c3ccc(Cl)cc3)sc2n(C)c1=O
Reaction #92189
methyl 3-(6-(4-chlorophenyl)-1,5-dimethyl-2,4-dioxo-1,2-dihydro thieno[2,3-d]pyrimidin-3(4H)-yl)propanoate
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCN(c2ccc(-n3cnc4cc(Br)sc4c3=O)cc2)C1
Reaction #159388
6-Bromo-3-[4-((R)-3-dimethylaminopyrrolidin-1-yl)phenyl]-3H-thieno[3,2-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCN(c2ccc(-n3cnc4cc(N5CCCCC5)sc4c3=O)cc2)C1
Reaction #159394
3-[4-((R)-3-Dimethylaminopyrrolidin-1-yl)phenyl]-6-piperidin-1-yl-3H-thieno[3,2-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Oc1c2cc(Br)sc2c(O)c2cc(Br)sc12
Reaction #163496
2,6-Dibromo-benzo[1,2-b:4,5-b′]dithiophene-4,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(O)c2ccc(Br)s2)cc1
Reaction #165244
title compound
Ausbeute 77.5%DOI: 10.6084/m9.figshare.5104873.v1
Oc1c2cc(Br)sc2c(O)c2cc(Br)sc12
Reaction #165574
2,6-Dibromo-benzo[1,2-b:4,5-b′]dithiophene-4,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCc1cccnc1)c1ccc(C#Cc2cnn3c(C(F)F)cc(-c4ccc(C(F)(F)F)cc4)nc23)s1
Reaction #176601
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(-c2ccc(C(F)(F)F)cc2)s1)n1cccc1
Reaction #183890
DOI: 10.1039/C8SC04228D
Clc1ccnc(-c2ccc(Br)s2)c1
Reaction #187761
DOI: 10.1039/C8SC04228D
CC(C)C(C#N)(CCCN1CCN(CCOc2cccc(C#N)c2)CC1)c1cc(C#N)sc1Br
Reaction #189570
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1)c1ccc(Br)s1
Reaction #190543
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(Br)s1)N1CCCC1
Reaction #194613
DOI: 10.1039/C8SC04228D
CSc1sc(-c2ncco2)c2c1C(=O)CCC2
Reaction #198344
DOI: 10.1039/C8SC04228D
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