2-Furoyl chloride

CN(CCO)C(=O)c1ccco1
Reaction #3167
N-(2-hydroxyethyl)-N-methylfuranamide
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc(-c2ccccc2)nc(-c2cccc([N+](=O)[O-])c2)c1CN1CCN(C(=O)c2ccco2)CC1
Reaction #4785
6-methyl-5-[4-(2-furoyl)piperazin-1-ylmethyl]-4-(3-nitrophenyl)-2-phenylpyrimidine
المردود 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(NCCCSc1ccncc1)c1ccco1
Reaction #6216
desired compound
المردود 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4ccco4)c3C2=O)C(=O)N1
Reaction #10063
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-2-furylcarboxamide
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccco4)c3C2=O)C(=O)N1
Reaction #10079
product
المردود 88.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@H](NC(=O)c1ccco1)[C@H](Oc1ccc2c(cnn2-c2ccncc2)c1)c1ccccc1
Reaction #41415
title compound
المردود 65.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(-n2ncc3cc(O[C@H](c4ccccc4)[C@H](C)NC(=O)c4ccco4)ccc32)cc1
Reaction #41419
title compound
المردود 48.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=C(Nc1ccc2sc(C(=O)N[C@H]3CN4CCC3CC4)cc2c1)c1ccco1
Reaction #43756
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(F)c2oc(-c3ccco3)nc2c1C#N
Reaction #45638
compound
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)N(NC(=O)c1ccccc1)C(=O)c1ccco1
Reaction #49933
N'-t-butyl-N-benzoyl-N'-(2-furoyl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CN1CCN(C(=O)c2c(N3CCN(C(=O)c4ccco4)CC3)n(-c3ccccc3)c3ccccc23)CC1
Reaction #54487
2-[4-(2-furoyl)-1-piperazinyl]-1-phenyl-indole 3-carboxylic acid 4-methyl-piperazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCc1nc2c(N)nc3cccnc3c2n1CCCCNC(=O)c1ccco1
Reaction #75759
N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]-2-furamide
المردود 29.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(Nc1ccc(-c2ccc(NC(=O)c3ccco3)c([N+](=O)[O-])c2)cc1[N+](=O)[O-])c1ccco1
Reaction #78026
3,3′-dinitro-4,4′-di-2-furoylamino-biphenyl
المردود 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C1CCC(N2C(=O)c3ccc(CNC(=O)c4ccco4)cc3C2=O)C(=O)N1
Reaction #91739
furan-2-carboxylic acid [2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-amide
المردود 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(NC1(C(=O)O)CCCCC1)c1ccco1
Reaction #161000
title compound
المردود 237.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)C[C@H](NC(=O)c1ccco1)C(=O)N[C@H](CO)C(C)C
Reaction #161031
title compound
المردود 86.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NCCc1ccc2c(c1)OCO2)c1ccco1
Reaction #174869
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)N1C(=O)C(=C(OC(=O)c2ccco2)c2cccs2)c2cc(F)c(Cl)cc21
Reaction #175972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1cc(C(C)(C)C)ccc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)c1ccco1
Reaction #176118
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1CC=C(c2c[nH]c3ccc(NC(=O)c4ccco4)nc23)CC1
Reaction #178689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي