1,3-oxazol-2-amine

Clc1ccnc(Nc2ncco2)c1
Reaction #415
Ausbeute 0.5%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #416
Ausbeute 7.7%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #453
Ausbeute 49.6%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #454
Ausbeute 0.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #455
Ausbeute 2.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #456
Ausbeute 3.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #457
Ausbeute 0.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #458
Ausbeute 0.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #459
Ausbeute 3.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #460
Ausbeute 11.1%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #461
Ausbeute 2.0%750 AstraZeneca ELN dataset
Clc1ccnc(Nc2ncco2)c1
Reaction #462
Ausbeute 2.5%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #672
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #673
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1ccc(Nc2ncco2)nc1
Reaction #674
Ausbeute 0.0%750 AstraZeneca ELN dataset
O=C1O[C@@H](CNc2ncco2)CN1c1ccc(C2=CCOCC2)c(F)c1
Reaction #8280
title compound
Ausbeute 4.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CBr)Nc1ncco1
Reaction #281790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Nc1ncco1)C1c2ccccc2Oc2ccccc21
Reaction #479895
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
O=C(Nc1ncco1)C(CC1CCCC1)c1ccc(Cl)c(Cl)c1
Reaction #485684
3-cyclopentyl-2-(3,4-dichlorophenyl)-N-oxazol-2-yl-propionamide
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
O=C(Nc1ncco1)C(CC1CCCC1)c1ccc(Cl)c(Cl)c1
Reaction #517377
3-cyclopentyl-2-(3,4-dichlorophenyl)-N-oxazol-2-yl-propionamide
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
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