formamidine acetate

Oc1ncnc2cc(F)c(I)cc12
Reaction #6919
title compound
المردود 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NC(=O)Cn1cnc2cc(OCc3cccc(F)c3)ccc2c1=O
Reaction #7721
title compound
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #47895
N-substituted-6-(pyridin-2-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #47897
substituted 5,6,7,8-tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidines
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]cnc2c1CN(Cc1ccccc1)CC2
Reaction #47898
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCCOc1ccc(NC(=O)c2n[nH]c3c2-c2ncncc2CC3)cn1
Reaction #51714
5,7-dihydro-6H-pyrazolo[3,4-h]quinazoline-9-carboxylic acid [6-(3-diethylamino-propoxy)-pyridin-3-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1cc2[nH]cnc2c(F)c1Nc1ccccc1Cl
Reaction #60256
pure desired product
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1cc2[nH]cnc2c(Cl)c1Nc1ccccc1
Reaction #60312
clean desired product
المردود 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCc2c(sc3nc[nH]c(=O)c23)C1
Reaction #66790
title compound
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CCc2sc3nc[nH]c(=O)c3c2C1
Reaction #66837
title compound
المردود 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
FC(F)(F)c1nc[nH]n1
Reaction #69016
3-(Trifluoromethyl)-1H-1,2,4-triazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1c2c(nc[nH]c2=O)CN1C(=O)OC(C)(C)C
Reaction #73371
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=c1[nH]cnc2c1CSC2
Reaction #73424
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)C(=O)O.OCCCc1c[nH]cn1
Reaction #77858
3-(1H-imidazol-4-yl)propanol oxalate
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1[nH]cnc1CCO.O=C(O)C(=O)O
Reaction #77859
2-(5-methyl-1H-imidazol-4-yl)ethanol oxalate
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Oc1ncnc2cc(F)c(I)cc12
Reaction #79377
title compound
المردود 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1cncc2c(O)ncnc12
Reaction #88232
title compound
المردود 56.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cn2ncnc(N)c2c1-c1ccc(NC(=O)OC(C)(C)C)c(F)c1
Reaction #160840
title compound
المردود 80.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1cc2c(N)ncnn2c1
Reaction #160848
above compound
المردود 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ncnn2cc(Br)cc12
Reaction #160869
desired compound
المردود 75.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
الصفحة 1التالي