2-aminoethanethiol

CCOC(=O)C1CSCCN1
Reaction #1569
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ccc(C2NCCS2)cn1
Reaction #50501
2-(2-chloro-5-pyridyl)thiazolidine
المردود 89.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Br.NCCSCc1nscc1Br
Reaction #55146
4-bromo-3-[(2-aminoethyl)thiomethyl]isothiazole hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Br.NCCSCc1nscc1Br
Reaction #55392
4-bromo-3-[(2-aminoethyl)thiomethyl]isothiazole hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Br.NCCSCc1nscc1Br
Reaction #55819
4-bromo-3-[(2-aminoethyl)thiomethyl]isothiazole hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
NCCSCc1nsc(Cl)n1
Reaction #55842
3-[(2-aminoethyl)thiomethyl]-5-chloro-1,2,4-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
NCCSCc1csnn1
Reaction #55843
4-[(2-aminoethyl)thiomethyl]-1,2,3-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1snnc1CSCCN
Reaction #55844
4-[(2-aminoethyl)thiomethyl]-5-methyl-1,2,3-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc[n+](-c2nc3ccc(C(F)(F)F)cc3[nH]2)c1CSSCCN.[Cl-]
Reaction #63760
2-[[(2-aminoethyl)dithio]methyl]-3 -methyl-1-[5-(trifluoromethyl)-2-benzimidazolyl1pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1cc(C)c(CSSCCN)[n+](-c2nc3ccc(C(F)(F)F)cc3[nH]2)c1.[Cl-]
Reaction #63762
2-[[(2-aminoethyl)dithio]methyl]-3,5-dimethyl-1 -[5-(trifluoromethyl)-2-benzimidazolyl]pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCCCn1c(=O)c(C2NCCS2)c(OC)c2cc(C)ccc21
Reaction #64325
1-Hexyl-3-(2-thiazolidinyl)-4-methoxy-6-methyl-2(1H)-quinolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CS(=O)(=O)O[C@@H]1C[C@@H](C2=NCCS2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65535
(2S,4R)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)-2-(2-thiazolin-2-yl) pyrrolidine
المردود 41.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)N1CCSC1c1nsc2ccc(-n3c(=O)cc(C(F)(F)F)n(C)c3=O)cc12
Reaction #77291
title compound
المردود 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C1CSCCN1
Reaction #80696
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cc(=O)[nH]c(Cc2cccnc2)n1
Reaction #96156
6-methyl-3-pyridylmethyl-4-pyrimidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1cc(C2NCCS2)ccc1O
Reaction #175096
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(C(=O)O)NCCS1
Reaction #177047
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #178412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NCCSCc1c[nH]c(N)n1
Reaction #180508
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSC(=C[N+](=O)[O-])NCCSCc1c[nH]c(N)n1
Reaction #183318
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي