An 16 Reaktionen beteiligt

16704

CCOC(=S)Nc1nc2ccc(Oc3ccc(F)cc3)cc2s1
Reaction #9231
desired compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Nc1ccc(O)cc1)N(CCCl)CCCl
Reaction #438315
28
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CN(C(=O)CCc1ccc(O)cc1)N(CCCl)CCCl
Reaction #438316
29
Ausbeute 19.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
COC(=O)C(Cc1ccc(O)cc1)NC(=O)N(CCCl)CCCl
Reaction #438317
30
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(=S)OC1CCN(C)C(=O)N1c1nnc(C)s1
Reaction #528654
tetrahydro-1-(5-methyl-1,3,4-thiadiazol-2-yl)-3-methyl-6-methylthiocarbonyloxy-2(1H)-pyrimidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_08
CSC(=O)NCc1c[nH]c2ccccc12
Reaction #733122
crude brownish-orange solid
Ausbeute 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
COC(=S)P(=O)(OC)OC
Reaction #752894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)C[C@@H]1C(=O)N(CC(=O)O)CCN1C(=O)[C@H](CC(=O)N1CCN(c2ccncc2)CC1)NC(C)=S
Reaction #1153754
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
COC(=S)N=C(N)SC
Reaction #1164251
methyl N-(1-amino-1-methylthiomethylene)thiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_05
COC(=S)P(=O)(OC)OC
Reaction #1366131
yellow oil
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CSC(=O)Nc1cc(-c2cc3ccccc3s2)c2[nH]ncc2c1
Reaction #1765430
(7-benzo[b]thiophen-2-yl-1H-indazol-5-yl)-thiocarbamic acid S-methyl ester
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
CSC(=O)N1c2ccccc2C(=O)N(C(C)C)S1(=O)=O
Reaction #1793965
S-methyl 3,4-dihydro-3-(1-methylethyl)-4-oxo-1H-2,1,3-benzothiadiazine-1-carbothioate-2,2-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_06
C[SH]=C(N)c1cccc(N2C(=O)CC(C)(C)C2=O)c1
Reaction #2069259
N(m-S-methylthiocarbamylphenyl)-2,2-dimethylsuccinimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_06
COC(=S)P(=O)(OC)OC
Reaction #2393305
yellow oil
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_08
CSC(=O)OC1=C(c2ccccc2I)S(=O)(=O)N(CC(F)F)c2ncsc21
Reaction #2446908
O-[1-(2,2-difluoroethyl)-3-(2-iodophenyl)-2,2-dioxido-1H-[1,3]thiazolo[4,5-c][1,2]thiazin-4-yl] S-methyl thiocarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
COc1cc(-c2csc3c(NC(=O)N4CCN(CCO)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #2477863
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09