glutaric anhydride

O=C(O)CCCC(=O)O.O=C1CCC(=O)N1O
Reaction #6431
mono N-hydroxysuccinimide glutarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)CCCC(=O)O)CC2)c1
Reaction #42606
5-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[1-(3-ethylphenyl)cyclopropyl]amino}-2-hydroxypropyl)amino]-5-oxopentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#Cc1cccc(NC(=O)CCCC(=O)O)c1
Reaction #47736
product
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#Cc1ccc(NC(=O)CCCC(=O)O)cc1
Reaction #47737
yellow white product 24
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CCCC(=O)O.O=C1CCC(=O)N1
Reaction #53751
succinimide glutarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cn1c(=O)c2[nH]cnc2n(C)c1=O
Reaction #56342
Theophylline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)CCCC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #67564
acid 151
收率 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCCC(=O)O
Reaction #92999
above-identified compound
收率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)CCCC(=O)Nc1ncc([N+](=O)[O-])s1
Reaction #163948
5-(5-nitrothiazol-2-ylamino)-5-oxopentanoic acid
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)CCCC(=O)N1CCN(c2cc3c(cc2F)c(=O)c(C(=O)O)c2sccn23)CC1
Reaction #180222
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C1CCC(=O)N2c3cc(Br)c(F)cc3Oc3ccccc3C12
Reaction #183740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCC(=O)O
Reaction #186635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1C(=O)CCCC(=O)O
Reaction #192457
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCC(=O)N1c1ccncc1
Reaction #214454
1-(4-pyridyl)-piperidine-2,6-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=C1CC(C(F)(F)F)CC(=O)N1c1ccc(Br)cc1
Reaction #226102
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCN1CCN(C(=O)CCCC(=O)O)CC1
Reaction #229003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)CCCC(=O)c1ccc2[nH]c(=O)[nH]c2c1
Reaction #229697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CCCC(=O)N1c1ccncc1
Reaction #231382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=Cc1ccccc1NC(=O)CCCC(=O)O
Reaction #238462
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCC(C)NC(=O)C=C(C)c1cccc(NC(=O)CCCC(=O)O)c1
Reaction #243594
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
第 1 页下一页