azetidine

N#Cc1ccc(N2CCC2)cc1
Reaction #527
Ausbeute 62.0%750 AstraZeneca ELN dataset
CN1CC(CCN2CCC2)Oc2ncccc2C1=O.O.O=C(O)C(=O)O
Reaction #4956
2-[2-(1-Azetidinyl)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one oxalate hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCN2CCC2)Oc2ncccc2C1=S.O=C(O)/C=C/C(=O)O
Reaction #4957
pale yellow crystals
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCN2CCC2)Oc2ncc(Cl)cc2C1=O.O=C(O)C(=O)O
Reaction #4959
2-[2-(1-Azetidinyl)ethyl]-7-chloro-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepin-5(4H)-one oxalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCN2CCC2)Oc2ncc(Cl)cc2C1=S.O=C(O)C(=O)O
Reaction #4961
yellow crystals
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)OC1(C(c2cc(F)cc(F)c2)S(C)(=O)=O)CN(C(c2ccccc2)c2ccccc2)C1
Reaction #46347
3-acetoxy-1-benzhydryl-3-[(3,5-difluorophenyl)(methyl-sulfonyl)methyl]azetidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(c1ccc(F)cc1)N1CCC1
Reaction #48862
solid
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCC2)cc1
Reaction #57814
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=c1c(-c2cccnc2)c[nH]n1-c1cc(N2CCC2)ncn1
Reaction #66186
2-(6-Azetidin-1-ylpyrimidin-4-yl)-4-pyridin-3-yl-1,2-dihydro-3H-pyrazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(/C=C/CN1CCC1)N1CCc2c(sc3ncnc(Nc4ccc(Cl)c(Cl)c4)c23)C1
Reaction #66852
title compound
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)c1cc(F)c2c(c1)OC(CN1CCC1)CO2
Reaction #67216
1-{[5-FLUORO-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}AZETIDINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)c1cc(Cl)c2c(c1)O[C@@H](CN1CCC1)CO2
Reaction #67230
1-{[(2S)-5-CHLORO-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}AZETIDINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)c1ccc2c(c1)OC(CN1CCC1)CC2
Reaction #67254
1-{[7-(METHYLSULFONYL)-3,4-DIHYDRO-2H-CHROMEN-2-YL]METHYL}AZETIDINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N
Reaction #69309
ammonia
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc(N2CCC2)ccc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)C[C@@H]1C.Cl
Reaction #71698
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CCN1C(=O)c1ccc(N2CCC2)nc1.Cl
Reaction #71702
title compound
Ausbeute 83.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(N2CCC2)ncc1C(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)C[C@@H]1C
Reaction #71706
title compound
Ausbeute 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1ccc(C(CN2CCC2)c2ccc(-c3cn[nH]c3)cc2)cc1
Reaction #73788
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1nc2c(cc1N1CCC1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76793
(R)-(−)-5′-(1-Azetidinyl)spiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
c1nc2c(cc1N1CCC1)C[C@@]1(CN3CCC1CC3)O2
Reaction #77890
(R)-(−)-5′-(1-Azetidinyl)spiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
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