chloride

Cc1c(F)c(F)cc(F)c1C(=O)Cl
Reaction #1369
2-methyl-3,4,6-trifluorobenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3149
solution
収率 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(=O)N(C)C)[N+](C)(C)C3)C[C@H]12
Reaction #5157
title compound
収率 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C1=C(CSCc2cccnc2)NC(C)=C(C#N)C1c1cccc([N+](=O)[O-])c1
Reaction #5744
(-)-2-(3-pyridinylmethylthio)methyl-5-cyano-3-carboethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)C1CCN(C(N)=S)C1
Reaction #7914
3-dimethylamino-pyrrolidine-1-carbothioic acid amide
収率 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(CC2=Cc3ccccc3C2)cc1
Reaction #12063
2-(4-fluorophenylmethyl)indene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1csc(-c2nn3c(Cc4ccc5c(c4)OCO5)nnc3s2)c1
Reaction #40720
compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nccn2COCC)c1
Reaction #42351
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #45024
solid
収率 4.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]ccc2onc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45522
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)=CCC/C(C)=C/CCCCO
Reaction #50482
title compound
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
N[C@H]1CC[C@H](C(=O)N2Cc3ccc(CN4CCOCC4)cc3C2)CC1
Reaction #51227
trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)CC(=O)O[CH2][Na]
Reaction #55676
Sodiomethylacetoacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CN(C)CCOC(=O)Cc1ccc(OCc2ccccc2)c(Cl)c1.Cl
Reaction #55883
β-dimethylaminoethyl 3-chloro-4-benzyloxyphenylacetate hydrochloride
収率 131.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
COC(OC)[C@]1(C)Oc2ccc(NC(=O)c3ccccc3)cc2[C@H](n2c(=S)oc3ccccc32)[C@H]1O
Reaction #57313
target compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc2c(c1)OCCC2N=[N+]=[N-]
Reaction #60329
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CCc1ccccc1)CN1CCCn2c1nc(-c1ccncc1)c(-c1cccc(C(F)(F)F)c1)c2=O
Reaction #62259
product
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCCCCC(=O)Nc1ccccc1C(=O)O
Reaction #64590
N-n-octanoylanthranilic acid
収率 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1cc2c(cc1C(=O)Cl)CCC2
Reaction #65218
5-methoxyindan-6-carboxylic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC1CCc2ccccc2SC1
Reaction #65700
2,3,4,5-tetrahydro-3-methyl-1-benzothiepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
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