N-benzyloxycarbonyl-S-methylisothiourea

CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #954
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #955
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #965
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #428981
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #428982
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #428990
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)n1nc(NC(=O)OCc2ccccc2)nc1-c1nc2c(s1)CCOc1cc(Br)ccc1-2
Reaction #795015
[5-(8-Bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-2-yl)-1-isopropyl-1H-[1,2,4]triazol-3-yl]-carbamic acid benzyl ester
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)[C@@H](CCNC(=N)NC(=O)OCc1ccccc1)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #934502
benzyl [N-[(3S,5S,6S)-6-[[N-[N-(t-butoxycarbonyl)-3-phenyl-L-alanyl]-L-histidyl]amino]-7-cyclohexyl-5-hydroxy-3-isopropylheptyl]amidino]carbamate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_08
CC(C)n1nc(NC(=O)OCc2ccccc2)nc1-c1nc2c(s1)CCOc1cc(Br)ccc1-2
Reaction #1277474
[5-(8-Bromo-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-2-yl)-1-isopropyl-1H-[1,2,4]triazol-3-yl]-carbamic acid benzyl ester
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
CC(C)C(CCNC(=N)NC(=O)OCc1ccccc1)CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #1327465
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(C)(C)OC(=O)C(C(=N)N)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #1502858
tert-butyl 4-CBZ-amidinopiperazin-1-ylacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #1537884
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #1537885
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1537895
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #1672665
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #1672666
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1672676
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
CC(C)(C)OC(=O)NCC1CCN(C(=N)NC(=O)OCc2ccccc2)CC1
Reaction #1697982
title product
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCO)CC1
Reaction #1697983
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #1697993
title compound
Ausbeute 67529.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
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