1-(6-bromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea

CCNC(=O)Nc1nc2cccc(O)c2s1
Reaction #9207
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OCc3ccccc3)c2s1
Reaction #9208
desired compound 9
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OC)c2s1
Reaction #9209
desired compound 10
المردود 2.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OC(C)C)c2s1
Reaction #9210
desired compound 11
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OCCOCCOC)c2s1
Reaction #9211
desired compound 12
المردود 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OCc3ccc(F)cc3)c2s1
Reaction #9212
desired compound 13
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(S(=O)(=O)C(F)(F)F)c2s1
Reaction #9213
1-(6-Bromo-7-trifluoromethanesulfonyl-2-benzthiazolyl)-3-ethyl-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2c(Br)cc(Br)c(O)c2s1
Reaction #9215
1-(4,6-Dibromo-7-hydroxy-2-benzothiazolyl)-3-ethyl-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OCc3ccccc3)c2s1
Reaction #230586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCNC(=O)Nc1nc2ccc(Br)c(OC)c2s1
Reaction #293840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCNC(=O)Nc1nc2ccc(Br)c(OC(C)C)c2s1
Reaction #373507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCNC(=O)Nc1nc2cccc(O)c2s1
Reaction #778299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCNC(=O)Nc1nc2ccc(Br)c(OCCOCCOC)c2s1
Reaction #1044387
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D