sodium triacetoxyborohydride

CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCC(F)(F)CN1CCOCC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6981
title compound
收率 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCN(C)Cc1nnc(C2CCN(c3ccccn3)CC2)n1Cc1ccccc1
Reaction #7015
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cnc2c(c1)CCCC2NCc1ccc(CN(Cc2ccccn2)C(=O)OC(C)(C)C)cc1
Reaction #7234
{4-[(3-methoxy-5,6,7,8-tetrahydroquinolin-8-ylamino)-methyl]-benzyl}-pyridin-2-ylmethyl-carbamic acid tert-butyl ester
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(CNC2CCCc3cccnc32)cc1
Reaction #7237
N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamine
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCc1ccc(CNCc2ccc(CN(Cc3nc4ccccc4[nH]3)C3CCCc4cccnc43)cc2)nc1
Reaction #7238
N-(5-butyl-2-pyridinylmethyl)-N′-(1H-benzimidazol-2-ylmethyl)-N′-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccccc1CNCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #7245
amine
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1cnc(CNCc2ccc(CN(Cc3nc4ccccc4[nH]3)C3CCCc4cccnc43)cc2)c(Cl)c1
Reaction #7254
amine
收率 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ncccc1CO
Reaction #7265
desired product
收率 151.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccccc1C(C)NCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #7266
desired product
收率 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cnc2c(c1)CCCC2N(Cc1ccc(CNCC2CCCN2)cc1)Cc1nc2ccccc2[nH]1
Reaction #7269
(1H-Benzoimidazol-2-ylmethyl)-(4-{[(pyrrolidin-2-ylmethyl)-amino]-methyl}-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(c1ccccc1)N(Cc1cccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)c1)Cc1ccccn1
Reaction #7274
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cnc2c(c1)CCCC2N(Cc1ccc(CNc2cc[nH]n2)cc1)Cc1nc2ccccc2[nH]1
Reaction #7276
amine
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc2c(c1)CCN(Cc1ccc(CN(Cc3nc4ccccc4[nH]3)C3CCCc4cccnc43)cc1)C2
Reaction #7277
foam
收率 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCc1ccc(CNc2ccccn2)cc1
Reaction #7281
title compound
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N[C@H]1CCCC[C@H]1Nc1ccccc1
Reaction #7285
cis-N-phenyl-N′-(t-butyloxycarbonyl)-cyclohexane-1,2-diamine
收率 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)N[C@@H]1CN(Cc2ccccc2)CC[C@@H]1C
Reaction #7306
Cis-(1-Benzyl-4-methyl-piperidin-3-yl)-carbamic acid methyl ester
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cc1ccc(F)cc1)N1CC(N2CCOCC2)CN1C(=O)OCc1ccccc1
Reaction #7739
desired product
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #8838
ketone-alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(C)Cc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #9030
title compound
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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