α-chloroethyl chloroformate

CC(Cl)OC(=O)OC(C)(C)C
Reaction #4521
α-chloroethyl tert-butyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(Cl)OC(=O)Oc1cccc2c1OC(C)(C)C2
Reaction #4524
1-chloroethyl 2,3-dihydro-2,2-dimethyl-7-benzofuranyl carbonate
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1Nc2c(ccc3c2CCNC3)C1=O
Reaction #5034
6,7,8,9-tetrahydro-1H-pyrrolo[2,3-f]isoquinoline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNCC(Cl)=C1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2OC)CC1.O=C(O)C(F)(F)F
Reaction #43783
72
Выход 27.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(c1ccc(Nc2ncnc3c2CNCC3)cc1)C(F)(F)F
Reaction #47911
product
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1.Cl.Cl
Reaction #53056
(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-2-indolinone-dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1.Cl.Cl
Reaction #53098
(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone-dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(Nc1cccc(C(=O)C2CCNCC2)n1)c1c(F)cc(F)cc1F
Reaction #58497
title compound
Выход 29.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #58515
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1sc2c(c1Br)CC1CNCC21
Reaction #58529
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1csc2c1C(C)C1CNCC21
Reaction #58537
6,7-Dimethyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[α]pentalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1cc2c(s1)CC1CCNCC21
Reaction #58551
subtitle compound
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1cc2c(s1)C1CNCCC1C2
Reaction #58555
subtitle compound
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1cc2c(s1)C1CCNCC1C2
Reaction #58559
subtitle compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)CC(O)(Cc1cc(F)ccc1-c1ccccc1)C1CNCCO1.Cl
Reaction #58603
40
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #58604
base
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cl.OC(Cc1ccccc1-c1ccccc1)(C1CCOCC1)C1CNCCO1
Reaction #58607
56
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(Cl)OC(=O)NCC1(CC(=O)OCc2ccccc2)CCCCC1
Reaction #58791
title compound ( 9 )
Выход 100.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOC(=O)CC1(CNC(=O)OC(C)Cl)CCCCC1
Reaction #58794
desired product ( 14 )
Выход 100.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)CC(CNC(=O)OC(C)Cl)CC(=O)OCc1ccccc1
Reaction #58802
title compound ( 40 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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