thionyl chloride

COC(=O)CCC(Cl)C(=O)Cl
Reaction #1874
2-chloro-4-methoxycarbonyl butyryl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(O)(C(=O)Nc1cccc2c1C(=O)c1ccccc1CO2)C(F)(F)F
Reaction #1919
Compound 1
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(O)(C(=O)Nc1cccc2c1C(=O)c1sccc1CO2)C(F)(F)F
Reaction #1920
Compound 7
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCS(=O)(=O)Cc1ccc(C(Cl)c2ccc(Cl)cc2)cc1
Reaction #2200
desired product
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2=O)cc1
Reaction #2346
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1cnc(OCCOc2ncnc(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)c2Oc2cccc(OC)c2)nc1
Reaction #2372
4-tert-butyl-N-[6-{2-(5-ethylpyrimidin-2-yloxy)ethoxy}-5-(3-methoxyphenoxy)pyrimidin-4-yl]benzenesulfonamide
収率 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCCC(=O)Nc1cccc(C(=O)OC)c1
Reaction #2430
oil
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1ccc(C(CC#N)N2C(=O)c3ccccc3C2=O)cc1OCC
Reaction #2447
product
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc(C#N)cc1
Reaction #2512
title compound
収率 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2554
title compound
収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cl)c1cc(F)c(F)c(F)c1F
Reaction #3055
2,3,4,5-tetrafluorobenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3079
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3080
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCCCC(Cl)CCCl
Reaction #3081
(-)-6,8-dichloro-octanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCCCC(Cl)CCCl
Reaction #3082
(+)-6,8Dichloro-octanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Cl)CCC(=O)c1ccc(C(=O)C2(O)CCCCC2)cc1
Reaction #3175
1-hydroxycyclohexyl 4-(2-chloroformylethyl)carbonylphenyl ketone
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1=C(C(=O)Cl)Cc2ccccc21
Reaction #3493
3-methylindene-2-oyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCNc1nc2nc(N)ncc2cc1-c1ccccc1
Reaction #3507
title compound
収率 44.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(-c2cc3cnc(N=CN(C)C)nc3nc2Cl)cc1
Reaction #3508
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccccc1C(=O)Nc1ccc(C(=O)Cl)cc1
Reaction #3593
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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