diisopropylether

CCc1cc(N[C@H]2CC[C@@H](C(C)(C)CC(C)(C)C)CC2)c(Br)cn1
Reaction #1120
2-Ethyl-4-[cis-4-(1,1,3,3-tetramethylbutyl)cyclohexylamino]-5-bromopyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #1177
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(OC)c1NC(=O)CNC(=O)OC(C)(C)C
Reaction #3019
N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nnc(-c2ccc(OC)cc2)n1-c1ccc(OC)cc1.Cl
Reaction #4690
3,4-bis-(4-methoxyphenyl)-5-ethyl-4H-1,2,4-triazole hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCc1nnc(-c2ccc(OC)cc2)n1-c1ccccc1.Cl
Reaction #4691
3-ethyl-5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccc(CS[C@H]2CCNC2)cc1.Cl
Reaction #5185
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CC(CCN2CCCC2)=NC=C1OCc1ccccc1
Reaction #5610
5-benzyloxy-2-[2-(1-pyrrolidinyl)ethyl]4-pyridone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Oc1cnc(C(=O)Cl)cc1OC(C)=O.Cl
Reaction #5616
4,5-diacetoxy-2-pyridinecarbonyl chloride hydrochloride
収率 158.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+]3(C)CCN(C(=O)c4cc(O)c(O)cn4)CC3)CS[C@H]12)c1nsc(N)n1
Reaction #5626
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-[1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)-1-piperazinio]methyl-3-cephem-4-carboxylate
収率 3.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)c1nc(CO)n(Cc2ccncc2)c1Sc1cc(Cl)cc(Cl)c1
Reaction #8507
compound ( 12 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N=C(NCC(=O)N[C@H]1CCNC1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=S(=O)(O)OS(=O)(=O)O
Reaction #10041
title compound
収率 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(C)C=CC(=O)c1cncnc1
Reaction #42044
objective compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC1(OC)CCNCC1.Cl
Reaction #49263
4,4-dimethoxypiperidine hydrochloride
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49601
4-chloro-5-(3-aminopropoxy)-7-iodoisoindolinone hydrochloride
収率 193.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.Nc1nc(C(=NOCF)C(=O)Cl)ns1
Reaction #50757
title compound
収率 106.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cn1nc(C(F)(F)F)cc1Oc1cc(Oc2cc(C(F)(F)F)nn2C)nc(Oc2cc(C(F)(F)F)nn2C)c1
Reaction #51597
colorless crystals
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)CCC(O)CC(=O)OCc1ccccc1
Reaction #53261
benzyl 6-methyl-3-hydroxyheptanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCNC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(-c4nc(N)c(F)cc4F)c3c2Br)C1
Reaction #53453
title compound
収率 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=S(=O)(Oc1ccc2[nH]ncc2c1)c1cccc(F)c1
Reaction #53654
1H-indazol-5-yl 3-fluorobenzenesulfonate
収率 59.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)n1ncc2cc(OS(=O)(=O)c3cccc(F)c3)ccc21
Reaction #53655
1-acetyl-1H-indazol-5-yl 3-fluorobenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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