部分構造検索

CC1(C)CCCNC1.Cl

CNc1cc(OC)c(C(=O)NCC23CCCN(CCC2)C3)cc1Cl
Reaction #5474
colorless crystals
収率 73.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(N3CCCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1.O=C(c1ccccc1)N1CCCC(CCCN2CCC(N3CCCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78337
1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(4-piperidinopiperid-1-yl)propyl]-piperidine Dihydrochloride Hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)C1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78338
expected product
収率 80.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1nc(C2(c3ccccc3)CCN(CCCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4ccccc4)C3)CC2)cs1.O
Reaction #78339
expected product
収率 104.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl.O.O
Reaction #78340
expected product
収率 132.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.O
Reaction #78341
expected product
収率 105.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.CCOC(=O)NC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl.Cl.O
Reaction #78344
expected product
収率 83.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(Cc3ccccc3)(C(=O)N3CCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1.O=C(c1ccccc1)N1CCCC(CCCN2CCC(Cc3ccccc3)(C(=O)N3CCCC3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78345
expected product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(OCCO)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78349
expected product
収率 128.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78350
expected product
DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1
Reaction #78351
expected product
収率 74.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #176060
DOI: 10.1039/C8SC04228D
COC(=O)CC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CNS(=O)(=O)c2cccs2)C2CC2)C1=O
Reaction #177245
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)C1CCC(=O)C1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)C(C)(C)C1
Reaction #180421
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cncc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #180857
DOI: 10.1039/C8SC04228D
CCOC(=O)CNC(=O)Nc1cccc(C(=O)NC(C(=O)N2CCC(O)(c3ccc(Cl)cc3)C(C)(C)C2)C(C)C)c1
Reaction #181498
DOI: 10.1039/C8SC04228D
COC(C)[Si](C)(C)C
Reaction #182548
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)CCl)C(=O)N1CCC(O)(c2ccc(Cl)cc2)C(C)(C)C1
Reaction #182971
DOI: 10.1039/C8SC04228D
CCC1(CC=O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CNS(=O)(=O)C2CC2)C2CC2)C1=O
Reaction #186555
DOI: 10.1039/C8SC04228D
CNc1cc(OC)c(C(=O)NCC23CCCN(CCC2)C3)cc1Cl
Reaction #192388
DOI: 10.1039/C8SC04228D
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