N-ethyl-N-propan-2-ylpropan-2-amine

Cc1ccccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1Cl
Reaction #3686
product
収率 106.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2n1Cc1ccccc1N(C(=O)c1ccc(NC(=O)c3ccc(Cl)cc3Cl)c(C)c1)C2
Reaction #3695
solid
収率 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CCCNC(=O)C(CSC(C)=O)Cc1ccccc1
Reaction #3852
(±)-4-[[2-[(Acetylthio)methyl]-1 oxo-3-phenylpropyl]amino]butanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)NNc1ccccc1OCCSC
Reaction #4340
2-[2-(methylthioethoxy)-phenyl]-hydrazinecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCc1ccc(N2CCC(CO)CC2)nn1
Reaction #5038
Formula IV
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cn1nnc(-c2ccc(OCc3ccccc3)cc2)n1
Reaction #5041
2-methyl-5-(4-benzyloxyphenyl)-2H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C1CCN(c2ccc(C)nn2)CC1
Reaction #5042
3-(4-carboethoxy-1-piperidinyl)-6-methylpyridazine
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCc1ccc(N2CCC(O)CC2)nn1
Reaction #5044
Formula IV
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)[C@H](C)[C@H]12
Reaction #5154
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3CC[N+](C)(C)C3)C[C@H]12
Reaction #5155
title compound
収率 18.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(=O)N(C)C)[N+](C)(C)C3)C[C@H]12
Reaction #5157
title compound
収率 22.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(S[C@H]3C[C@@H](C(N)=O)[N+](C)(C)C3)C[C@H]12
Reaction #5158
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON(C)C(C)CNc1ncnc2nc[nH]c12
Reaction #5370
white crystals
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
Reaction #5446
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(C=O)c(Br)c(Cl)c1OC
Reaction #5452
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc2c(c1)OC(CNCCCOc1ccc3c(=O)ccoc3c1)CO2
Reaction #5668
title compound
収率 4.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=c1ccoc2cc(OCCCNCC3COc4ccc(O)cc4O3)ccc12
Reaction #5669
title compound
収率 10.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)CC(=O)C[C@@H](CC#N)O[Si](C)(C)C(C)(C)C
Reaction #5779
(R)-1,1-dimethylethyl 6-cyano-5-[(1,1-dimethylethyl)dimethylsilyl]oxy-3-oxohexanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)[Si](C)(C)OCc1ccc(CBr)cc1
Reaction #6023
title compound
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCC(CO)C(O)c1cccnc1
Reaction #6532
(2S)-2-[(1S-1-hydroxy-1-(3-pyridyl)methyl]pent-4-enoyl)-4-isopropyloxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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