子结构搜索

802

COC(=O)C1CCN(c2ccc(F)c(C)c2)CC1

C#CCN1CCC(C(=O)OC)CC1

Reaction #44337

1-Prop-2-ynyl-piperidine-4-carboxylic acid methyl ester

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1(C)CCN(C(=S)Nc2ccc(Cl)cc2)CC1

Reaction #48554

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1CCN(Cc2ccc3c(c2)cc(-c2ccc(Cl)c4c2C(=O)NC4)n3C(=O)OC(C)(C)C)CC1

Reaction #49305

4-chloro-7-[1-(tert-butoxycarbonyl)-5-(4-methoxycarbonylpiperidinomethyl)indol-2-yl]isoindolinone

收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CC2CCCC(C1)N2

Reaction #49661

Ethyl-9-azabicyclo[3.3.1]nonane-3-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)CN1C2CCCC1C(C(=O)OCC)CC2

Reaction #49662

Ethyl-N-ethoxycarbonylmethyl-9-azabicyclo[3.3.1]nonane-4-carboxylate

收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCOC(=O)C1CCN(Cc2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)CC1$

Reaction #53155

(Z)-3-{1-[4-(4-ethoxycarbonyl-piperidinomethyl)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1(N(C(=O)Cc2ccc(Cl)cc2)c2ccccc2)CCN(C(C)C)CC1.O=C(O)C(=O)O

Reaction #55039

methyl 4-[N-(4-chlorophenyl)acetyl-N-phenylamino]-1-(1-methylethyl)-4-piperidinecarboxylate ethanedioate

收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1(N(C(=O)Cc2ccc(Cl)cc2)c2ccccc2)CCN(C(C)C)CC1.O=C(O)C(=O)O

Reaction #56431

methyl 4-[N-(4-chlorophenyl)acetyl-N-phenylamino]-1-(1-methylethyl)-4-piperidinecarboxylate ethanedioate

收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCN(C(C)C)CC1

Reaction #59062

ethyl-1-(methylethyl)piperidine-4-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1CCN(Cc2ccccc2)CC1

Reaction #70839

desired compound

收率 924.2%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1CCN(c2nc3ccc(OC)cc3cc2C(F)(F)F)CC1

Reaction #84094

收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1CCN(c2ccc([N+](=O)[O-])cc2)CC1

Reaction #85850

methyl 1-(4-nitrophenyl)piperidine-4-carboxylate

收率 58.6%DOI: 10.6084/m9.figshare.5104873.v1

O=C(O)C1CCN(c2ccc(Br)cc2)CC1

Reaction #85866

crude title compound

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCNC(=O)C1

Reaction #90750

ethyl 2-oxopiperidine-4-carboxylate

收率 94.5%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCNC(=S)C1

Reaction #90751

ethyl 2-thioxopiperidine-4-carboxylate

收率 49.3%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCn2c(nnc2C(F)(F)F)C1

Reaction #90752

ethyl 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine-7-carboxylate

收率 88.9%DOI: 10.6084/m9.figshare.5104873.v1

C=C(C#N)CN1CCC(C(=O)OCC)CC1

Reaction #94934

2-(4-Carboethoxy-1-piperidylmethyl)propenenitrile

DOI: 10.6084/m9.figshare.5104873.v1

C=C(C#N)CN1CCC(C(=O)OCC)CC1

Reaction #94944

2-(4-Carboethoxy-1-piperidylmethyl)propenenitrile

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCN(Cc2cccc(Nc3nc(Cl)ncc3F)c2)CC1

Reaction #158498

2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine

DOI: 10.6084/m9.figshare.5104873.v1

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