reactin

CC(=O)OCN(CN(CN(C)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
Reaction #5318
1-Acetoxy-2,4,6-trinitro-2,4,6-triazaheptane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cccc2c1cnn2C(C)C
Reaction #172710
title compound
المردود 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1CCC(=C2c3ccccc3CCc3ccccc32)CC1
Reaction #215817
4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidine
المردود 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CN1CCC(=C2c3ccccc3CCc3ccccc32)CC1
Reaction #400367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(Br)Cc1ccc(OCCn2c(CC)nc(C)cc2=O)cc1
Reaction #469470
title compound
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COCOc1cccc([C@@H](CO)N2CC[C@H](OCOC)C2)c1
Reaction #469496
2-(S)-(3-Methoxymethoxyphenyl)-2-(3-(S)-methoxymethoxypyrrolidin-1-yl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CN1CCN(CC2CNCCO2)CC1
Reaction #565002
2-(4-methyl-1-piperazinylmethyl) morpholine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
COC(=O)c1sc2ncnc(Nc3cccnc3OCC(C)F)c2c1C
Reaction #619474
Methyl-4-(2-(2-fluoropropoxy)pyridin-3-ylamino)-5-methyl-thieno[2,3-d]pyrimidine-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CS(=O)(=O)Oc1cc2c(cc1C(=O)CCCl)NC(=O)CC2
Reaction #1372603
6-methylsulfonyloxy-7-(3-chloropropionyl)-3,4-dihydrocarbostyril
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_01
COC(=O)c1ccc(C(=O)OC)c(-c2ccc(C)cc2)c1
Reaction #1581028
desired product
المردود 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_06
CCOC(=O)N1CCC(=C2c3ccccc3C=Cc3ccccc32)CC1
Reaction #1630543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCC1(CC)Oc2c(C(=O)O)sc(C(=O)O)c2OC1CO
Reaction #1760342
product
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Cl.O=S(=O)(c1ccc2c(c1)Cc1ccccc1-2)N1CCN(Cc2ccccc2)CC1
Reaction #1810006
title compound
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_08
CC(=O)Nc1cccc(Oc2cc3c(cn2)nc(CC#N)n3-c2ccc3c(c2)CN(C(=O)OC(C)(C)C)CC3)c1
Reaction #2073544
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
CN(C)c1ccc2c(c1)CCN(c1cccc(-c3cc(NC(=O)CC#N)c(=O)n(C)c3)c1CO)C2=O
Reaction #2157029
2-Cyano-N-{5-[3-(6-dimethylamino-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-2-hydroxymethyl-phenyl]-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl}-acetamide
المردود 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
CCOC(=O)C(Br)Cc1ccc(OCCn2c(CC)nc(C)cc2=O)cc1
Reaction #2298645
title compound
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_09
COC(=O)[C@@H]1C[C@H](NCc2cc(OC(F)(F)F)ccc2OC)[C@H](c2ccccc2)N(C(=O)OCc2ccccc2)C1
Reaction #2374717
oil
المردود 114.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_07
CN1CCC(=C2c3ccccc3CCc3ccccc32)CC1
Reaction #2381245
4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidine
المردود 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CCOC(=O)N1CCC(=C2c3ccccc3C=Cc3ccccc32)CC1
Reaction #2458887
pale yellow crystals
المردود 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_03