salicylamide

CN1CCC(Oc2ccccc2C(N)=O)C1
Reaction #4875
2-(1-Methyl-3-pyrrolidinyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.O
Reaction #4877
product
Yield 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1(C)NC(=O)c2ccccc2O1
Reaction #198677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NC2(CCN(Cc3ccccc3)CC2)Oc2ccccc21
Reaction #200047
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCOc1ccccc1C(N)=O
Reaction #206827
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)COc1ccccc1C(N)=O
Reaction #209709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)Oc1ccccc1C(N)=O
Reaction #216250
o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide
Yield 49.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
NC(=O)c1ccccc1OCC1CC1
Reaction #237334
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN1CCC(Oc2ccccc2C(N)=O)C1
Reaction #323303
2-(1-Methyl-3-pyrrolidinyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.O
Reaction #323305
product
Yield 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CN1CCC(Oc2ccccc2C(N)=O)C1
Reaction #334430
2-(1-Methyl-3-pyrrolidinyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.O
Reaction #334431
product
Yield 34.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
CCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)Oc1ccccc1C(N)=O
Reaction #344289
o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide
Yield 49.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CC1(C)NC(=O)c2ccccc2O1
Reaction #346407
2,2-dimethyl-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=C(O)c1ccccc1O
Reaction #349285
salicylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_05
CCCCCCCCCCOc1ccccc1C(N)=O
Reaction #372344
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CON1C(=O)CC2(CCN(CNC(=O)c3ccccc3O)CC2)C1=O
Reaction #392779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCCCCCCc1ccc2oc(-c3ccccc3O)nc2c1
Reaction #416373
2-(2-Hydroxyphenyl)-5-dodecylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CCCCCCc1ccc2oc(-c3ccccc3O)nc2c1
Reaction #416374
2-(2-Hydroxyphenyl)-5-hexylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CN1CCC(Oc2ccccc2C(N)=O)C1
Reaction #451540
2-(1-Methyl-3-pyrrolidinyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
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