methanol;hydrochloride

Cl.Cl.NCCCNc1cccc2nccn12
Reaction #5530
desired product
수율 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CS(=O)(=O)NCCSc1cccc2nccn12.Cl
Reaction #5535
desired product
수율 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.O=C1c2ccccc2C(=O)N1CCCOc1ccncc1
Reaction #6257
desired compound
수율 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
Reaction #6258
desired compound
수율 86.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.Cl.O=C(NCCCSc1ccncc1)c1cnccn1
Reaction #6272
desired compound
수율 85.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(=O)N(CCCCSc1ccncc1)c1ccccc1N(CCCCSc1ccncc1)C(=O)CC.Cl.Cl
Reaction #6284
desired product
수율 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOP(=O)(CO[C@@H](CO)CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)OCC
Reaction #6353
title compound
수율 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](C(=O)N1CCCCC1)N1CC[C@H](N(CC(=O)O)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7410
title compound
수율 205.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCN(CCCc1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10588
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCN(CCc1cccs1)S(=O)(=O)c1cccc2cnccc12
Reaction #10589
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCN(CCCCc1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10590
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cncc2cccc(S(=O)(=O)N(CCCN)CCCc3ccccc3)c12.Cl
Reaction #10591
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCN(CCS(=O)(=O)c1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10592
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCN(CCS(=O)(=O)c1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10593
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCN(CCCc1ccccc1)S(=O)(=O)c1cccc2c(N)nccc12
Reaction #10595
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCN(CCS(=O)(=O)c1ccccc1)S(=O)(=O)c1cccc2c(N)nccc12
Reaction #10596
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCOc1cccc2c(N)nccc12
Reaction #10599
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.Nc1nccc2c(OCC3CCCNC3)cccc12
Reaction #10600
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCNc1cccc2cnccc12
Reaction #10602
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.NCCCNc1cccc2cnccc12
Reaction #10603
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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