N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride

CC#C[C@H](C)Oc1cc(N)c(Cl)cc1C(=O)NC1C2CCC1CN(Cc1ccccc1)C2
Reaction #1032
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(I)nc1
Reaction #1321
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2ccc(C#Cc3ccc(C(=O)OCC[Si](C)(C)C)cc3)cc21
Reaction #1334
Trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)O.Cl.NCC(=O)Nc1nc2c(s1)CCN(C(=O)c1ccc(NC(=O)c3ccccc3-c3ccccc3)cc1)c1ccccc1-2
Reaction #1441
4'-[(2-glycylamino-5,6-dihydro-4H-thiazolo[5,4-d][1]benzazepin-6-yl)carbonyl]-2-phenylbenzanilide 2-propylalcohol hydrochloride
Yield 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(OC(=O)c2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
Reaction #1489
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(c2cccs2)c2cc(C(=O)Oc3ccc(C(=O)OCC[Si](C)(C)C)cc3)ccc21
Reaction #1490
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CN1C(=O)[C@@H](CC(N)=O)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1888
crystal
Yield 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1
Reaction #2002
N-(t-Butoxycarbonyl)-D-tryptophan benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1
Reaction #2003
(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]-1H-indole-3-propanoic acid, benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.NCCNC(=O)c1cc(-c2ccnc(Nc3cccc(Cl)c3)n2)ccn1
Reaction #2256
N-[3-chloro-phenyl]-4-[2-(N-{2-amino-ethyl}-aminocarbonyl)-4-pyridyl]-2-pyrimidineamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2517
title compound
Yield 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCN(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)C(=O)c1ccc(CNC(=O)[C@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #2605
title compound
Yield 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1ccccc1CC(C(=O)OCC[Si](C)(C)C)N1C(=O)c2ccccc2C1=O
Reaction #2808
title compound
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C(=O)N2CCOCC2)cc1[N+](=O)[O-]
Reaction #2831
crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1cccc([N+](=O)[O-])c1)N1CCOCC1
Reaction #2832
compound ( [13]-(132)-158 )
Yield 89.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@H]1CCNC1=O
Reaction #2840
title compound
Yield 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3141
hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1c2ccccc2C(c2ccccc2F)=NCC1CNC(=O)Cc1c[nH]c2ccccc12.O
Reaction #4275
oil
Yield 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Nc1nc2c(ncn2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)o1
Reaction #5242
oxanosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCCCCOc1ccc(Cl)cc1)C1=C(O)COC1=O
Reaction #5341
4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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