2-butylamino-4-methyloxazole

CCCCN(C(=O)C(C)C)c1nc(C)co1
Reaction #54761
2-(N-butylisobutyramido)-4-methyloxazole
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCN(C(=O)NCC)c1nc(C)co1
Reaction #75033
1-Butyl-3-ethyl-1-(4-methyl-2-oxazolyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCCCCCNC(=O)N(CCCC)c1nc(C)co1
Reaction #75034
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
C=CCNC(=O)N(CCCC)c1nc(C)co1
Reaction #75035
1-Allyl-3-butyl-3-(4-methyl-2-oxazolyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCCCN(C(=O)OCC)c1nc(C)co1
Reaction #75036
Ethyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCCCN(C(=O)NCC)c1nc(C)co1
Reaction #215412
1-Butyl-3-ethyl-1-(4-methyl-2-oxazolyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCCCNC(=O)N(CCCC)c1nc(C)co1
Reaction #215413
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
C=CCNC(=O)N(CCCC)c1nc(C)co1
Reaction #215414
1-Allyl-3-butyl-3-(4-methyl-2-oxazolyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCN(C(=O)OCC)c1nc(C)co1
Reaction #215415
Ethyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
C=CCNC(=O)N(CCCC)c1nc(C)co1
Reaction #270538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCN(C(=O)C(C)C)c1nc(C)co1
Reaction #777072
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCCN(C(=O)NCC)c1nc(C)co1
Reaction #924361
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCN(C(=O)C(C)C)c1nc(C)co1
Reaction #1199565
2-(N-butyl isobutyramido)-4-methyloxazole
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_10
CCCCN(C(C)=O)c1nc(C)co1
Reaction #1199572
2-(N-Butylacetamido)-4-methyloxazole
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_10
CCCCN(C(C)=O)c1nc(C)co1
Reaction #1288760
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCCCCNC(=O)N(CCCC)c1nc(C)co1
Reaction #2211031
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCCCN(C(=O)OCC)c1nc(C)co1
Reaction #2401920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)