Участвует в 559 реакциях

2779

CCCCNC(=O)Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(NC(=O)NCCCC)nc2n1

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

CCCCNC(=O)NS(=O)(=O)c1ccccc1CCl

Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

CCOc1ccc(C(=O)OC)c(S(=O)(=O)N=C=O)c1

methyl 4-ethoxy-2-(isocyanatosulfonyl)benzoate

Выход 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

COC(=O)c1ccc(SC)cc1S(=O)(=O)N=C=O

methyl 2-(isocyanatosulfonyl)-4-(methylthio)benzoate

Выход 111.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

COC(=O)C(C)Oc1ccccc1S(=O)(=O)N=C=O

2-(1-methoxycarbonylethoxy)benzenesulfonyl isocyanate

Выход 125.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

CCCCNC(=O)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1

N-Butyl-2-[[3-[3-(1-piperidinylmethyl) phenoxy]propyl]aminothioxomethyl]-hydrazine carboxamide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

CCCCNC(=O)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O

Reaction #10117

N-{[2-(2,6-dioxo(3-piperidyl))1,3-dioxoisoindolin-4-yl]methyl}(butylamino)carboxamide

Выход 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCCNC(=O)Nc1sc2c(c1C#N)CCCC2

Reaction #49645

2-(3-n-Butylureido)-3-cyano-4,5,6,7-tetrahydrobenzo[b]thiophene

Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06

$CCCCNC(=O)Nc1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1$

Reaction #53051

(Z)-3-[1-(4-butylaminocarbonylamino-phenylamino)-1-phenyl-methylidene]-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

CCCCNC(=O)Nc1cccc(N2CN=c3occc3=C2N)c1

Reaction #60759

4-Amino-3-(3-((butyl)aminocarbonylamino)phenyl)furo[2,3-d]pyrimidine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

CCCCNC(=O)NS(=O)(=O)c1c(SC)cccc1SC

Reaction #63150

Выход 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08

CCCCNC(=O)NCCCCn1c(CCCC)nc2c(N)nc3cccnc3c21

Reaction #75757

N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]-N′-butylurea

Выход 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

CCCCNC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94618

2-(7-chloro-1,8 naphtyridin-2-yl)-3-n-butylaminocarbonyloxy-isoindolin-1-one

Выход 46.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2cc(C(F)(F)F)ccc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94620

3-n-butylaminocarbonyloxy-2-(7-chloro-1,8-naphthyridin-2-yl)-5-trifluoromethyl-isoindolin-1-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2ccc(C(F)(F)F)cc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94622

2-(7-chloro-1,8-naphthyridin-2-yl)-3-n-butylaminocarbonyloxy-6-trifluoromethyl-isoindolin-1-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2cc(Cl)ccc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94623

5-chloro-2-(7-chloro-1,8-naphthyridin-2-yl)-3-n-butylaminocarbonyloxy-isoindolin-1-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2nccnc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94624

5-n-butylaminocarbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine

Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2cccnc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94625

5-n-butylaminocarbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)OC1c2ncccc2C(=O)N1c1ccc2ccc(Cl)nc2n1

Reaction #94626

7-n-butylaminocarbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-5-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

CCCCNC(=O)NS(=O)(=O)c1sccc1C

Reaction #179651

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

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