isoamyl alcohol

Cc1ccc(Nc2ccc3c4c(cccc24)CC3)cc1

5-[N-(4-tolyl)amino]acenaphthene

収率 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

CC(=O)NC1CCN(c2ccncc2)CC1

4-acetylamino-1-(4-pyridyl)piperidine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03

CC(C)(C)OC(=O)NCC1(O)CCN(c2cc[n+]([O-])cc2)CC1

Reaction #53317

収率 36.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

Nc1nc(NCCCCCCNS(=O)(=O)c2cccc3ccccc23)nc2ccccc12

Reaction #78809

naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

CNS(=O)(=O)Cc1ccc(Nc2nc(Nc3ccccc3)c3cc(OC)ccc3n2)cc1

Reaction #78817

N-methyl-[4-(6-methoxy-4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

CNS(=O)(=O)Cc1ccc(Nc2nc(Nc3ccccc3)c3ccccc3n2)cc1.Cl

Reaction #78819

N-methyl-[4-(4-phenylamino-quinazolin-2-ylamino)-phenyl]-methanesulfonamide hydrochloride

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03

OC[C@@H]1CC[C@H]2CN(c3ccccn3)CCN2C1

Reaction #80325

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04

CSc1cc2n(c1C(=O)c1ccccc1)CCC2C(=O)OCCC(C)C

Reaction #93363

isoamyl 5-benzoyl-6-methylthio-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09

$CC(C)CCOc1cc(-c2ccccc2)nc2nn(C)cc12.O=C(O)/C=C\C(=O)O$

Reaction #94269

2-Methyl-4-(3-methylbutoxy)-6-phenyl-2H-pyrazolo[3,4-b]pyridine maleate

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12

C=CC(=O)OCCC(C)C

Reaction #175413

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

OCC1CC2CN(c3ccc(Cl)cn3)CCN2C1

Reaction #179510

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCCCCCCCCCc1nc(Cl)cc(OCC(CC)CCCC)n1

Reaction #182281

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Fc1ccc(OCC2CC3CN(c4cncc(Cl)n4)CCN3C2)cc1

Reaction #189598

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(=O)OCCC(C)C

Reaction #197742

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(C)CCOC1Oc2ccc(OS(C)(=O)=O)cc2C1(C)C

Reaction #199777

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(C)CCOc1c(Cl)cnn(C(C)(C)C)c1=O

Reaction #199845

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Fc1ccc(OCC2CC3CN(c4ccc(Cl)nn4)CCN3C2)cc1

Reaction #200616

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction #204055

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

c1cc2c3c(c1)nc(N1CCC(c4c[nH]cn4)CC1)n3CCC2

Reaction #206480

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

COc1cc2nc(N3CCCC(N4C(=O)CC5(CCCC5)CC4=O)C3)nc(N)c2cc1OC.Cl

Reaction #214471

8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-3-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03

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