cyclobutylmethyl bromide

Cc1cc(C#Cc2cn(CC3CCC3)c(C)n2)ccn1

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

Cc1nc(C#Cc2ccnc(Cl)c2)cn1CC1CCC1

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1SCC1CCC1

Reaction #53556

2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile

Yield 21.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

C[C@@H]1CN(c2ccc(N3CCN(CC4CCC4)CC3)c(C3CCC(C)(C)CC3)c2)C[C@H](C)O1

Reaction #60458

cis-4-[4-(4-cyclobutylmethylpiperazin-1-yl)-3-(4,4-dimethylcyclohexyl)phenyl]-2,6-dimethylmorpholine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09

O=C1CC[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CCC2)[C@H]1O5

Reaction #67604

N-(cyclobutylmethyl)-noroxymorphone

Yield 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09

Fc1c(Nc2cc3c4c(c2)[C@@H]2CN(CC5CCC5)CC[C@@H]2N4CCOC3)cccc1C(F)(F)F

Reaction #75848

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

CCOC(=O)C(O)CC1CCC1

Reaction #85096

Ethyl 3-cyclobutyl-2-hydroxypropanoate

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09

O=C1c2ccccc2C(=O)N1CCCc1cccc(OCC2CCC2)c1

Reaction #161538

2-(3-(3-(cyclobutylmethoxy)phenyl)propyl)isoindoline-1,3-dione

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

$COc1ccc(Cl)cc1C(=O)/N=c1\sn(C(C)(C)C)cc1C(O)CC1CCC1$

Reaction #163439

Yield 53.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

$COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)=O)c(C)n1CC1CCC1$

Reaction #165705

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09

OCCNCC1CCC1

Reaction #179935

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

COc1ccc(S(=O)(=O)N2CCC3=Cc4c(cnn4-c4ccc(F)cc4)CC3(C(=O)OCC3CCC3)C2)cn1

Reaction #205834

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

CC(C)(C)OC(=O)N1CCC(OCC2CCC2)CC1

Reaction #227159

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

O=C1CN(Cc2ccc(Br)cc2)C(=O)N1CC1CCC1

Reaction #227978

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CC(C)N1CCN(C(=O)c2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3CC2CCC2)CC1

Reaction #228053

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CSc1ccc(C(O)(CC2CCC2)c2cc3cc(F)cnc3n2S(=O)(=O)c2ccccc2)cc1

Reaction #255035

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction #261437

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)

CC1(CC2CCC2)NC(c2ccccc2)COC1=O

Reaction #265893

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

O=C1c2ccccc2C(=O)N1CCCc1cccc(OCC2CCC2)c1

Reaction #276718

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

COc1ccc2c(c1)C13CCN(CC4CCC4)C(C2)C1C(C)CC(=O)C3

Reaction #278730

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

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