1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinol

O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7547
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol maleate
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7548
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7549
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)CC(O)(CC(=O)O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7550
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol citrate
Yield 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #649565
achromatic crystal
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #684992
achromatic crystal
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #1179958
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol maleate
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=[N+]([O-])OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #1179959
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #1179960
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C(O)CC(O)(CC(=O)O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #1179961
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol citrate
Yield 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C(CCOCCc1ccc2sccc2c1)N1CC(O)C1
Reaction #1225974
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=[N+]([O-])O
Reaction #1628479
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=C(CCOCCc1ccc2sccc2c1)N1CC(O)C1
Reaction #2464343
3-[2-(1-benzothiophen-5-yl)ethoxy]-1-(3-hydroxy-1-azetidinyl)-1-propanone
Yield 117.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2464345
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol maleate
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=[N+]([O-])OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2464346
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2464347
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=C(O)CC(O)(CC(=O)O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2464348
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol citrate
Yield 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2473267
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol maleate
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
O=[N+]([O-])OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2473268
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol nitrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #2473269
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
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