n-propyl isocyanate

CCCNC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10118
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(propylamino)carboxamide
Rendement 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)NC(=O)O.CCCNC(=O)C1(S(N)(=O)=O)CC1
Reaction #46082
1-propylcarbamoylcyclopropanesulfonamide tert-butylcarbamate
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nn(-c2cc(NC(=O)NCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64533
desired compound
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCNC(=O)NCC(C(=O)OC)c1cccc2ccccc12
Reaction #65566
N-[2-(1-naphthyl)-2-(methoxycarbonyl)ethyl]-N'-propylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #66234
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCNC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75629
title compound
Rendement 112.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCNC(=O)NCC(C(=O)OC)c1cccc2ccccc12
Reaction #80569
N-[2-(1-NAPHTHYL)-2-(METHOXYCARBONYL)ETHYL]-N'-PROPYLUREA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #81685
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCNC(=O)NCc1ccc2c(c1)CN(C1CCC(=O)NC1=O)C2=O
Reaction #91791
1-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-3-propyl-urea
Rendement 55.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCNC(=O)NCc1ccc2c(c1)C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #91798
1-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-3-propyl-urea
Rendement 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)NC(=O)N1CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162061
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCNC(=O)N1CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162062
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCNC(=O)NCCCCCN1CCC(CNC(=O)OC(C)(C)C)CC1
Reaction #180168
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCNC(=O)n1nc(Oc2ccc([N+](=O)[O-])cc2C(F)(F)F)cc1C
Reaction #182475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCNC(=O)N1CCC(c2nc(-c3ccncc3)no2)CC1
Reaction #183837
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCNC(=O)NCCc1ccc([N+](=O)[O-])cc1
Reaction #208297
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCNC(=O)Nc1nc(-c2cc(C)cc(C)c2)c(-c2ccncc2)s1
Reaction #222110
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCNC(=O)N1CC(c2ccc(F)cc2)C(N(C)C(=O)N(C)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C1
Reaction #228834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCN1C(=O)N(S(=O)(=O)c2ccccc2)CC1C(=O)N1CCN(c2cc(C)ccc2C)CC1
Reaction #235817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCNC(=O)Nc1cc(C(=O)OC)c(Br)cn1
Reaction #235988
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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