iodoethane

CCOC(=O)C[C@H]1O[C@H](c2ccc(OCC)cc2OC)c2cc(Cl)ccc2N(CC(C)(C)C)C1=O
Reaction #1907
ethyl trans-7-chloro-5-(4-ethoxy-2-methoxyphenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1cc(Cl)ccn1
Reaction #1945
title compound
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1cc(Cl)c(F)cn1
Reaction #1958
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1nc(F)c(F)c(F)c1F
Reaction #1966
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1cnc2c1c(=O)n(CC)c(=O)n2C
Reaction #2088
7-Ethoxymethyl-1-ethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCn1c(=O)c2c(ncn2CC)n(C)c1=O)OCC
Reaction #2119
Diethyl [4-(7-ethyl-3-methylxanthin-1-yl)butyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3037
desired title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(N)nc21
Reaction #3271
2-amino-6-(2,6-dichlorophenyl)-8-ethyl-pyrido[2,3-d]pyrimidin-7(8H)-one
Выход 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1cn(NC(C)C=O)c2cc(-n3cccc3)c(F)cc2c1=O
Reaction #4664
solid
Выход 37.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(N)=O
Reaction #5192
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1CC
Reaction #5198
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)NC
Reaction #5200
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C(NCc1cccc(C(F)(F)F)c1)c1cn(Cc2ccccc2)c2ccccc12
Reaction #5701
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(COc2ccc3c(c2)C(C)(C)CCC3(C)C)cc1
Reaction #6610
title compound
Выход 40.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC[N+]1(CC2(c3ccc(Cl)cc3)CC2)CCCC1.[I-]
Reaction #6663
1-[1-(4-chloro-phenyl)-cyclopropylmethyl]-1-ethyl-pyrrolidinium iodide
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCN1c2ccccc2Sc2ccccc21
Reaction #6673
10-Ethylphenothiazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCn1nc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(Cc2ccc(OC)cc2)c1C
Reaction #6748
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1ccc(Cc2c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)nn(CC)c2C)cc1
Reaction #6749
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1ccc(Cc2c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)nn(CC)c2C)cc1
Reaction #6750
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC1=c2ccccc2=NC1=O
Reaction #7081
title compound
Выход 2.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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