部分構造検索

CN1CCCC1

O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9491
1-[3-(7-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2ccc(Br)cc12
Reaction #9493
1-[3-(6-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
収率 87.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(-c3ccccc3)ccc12
Reaction #9506
1-[3-(3-nitro-7-phenylquinolin-4-ylamino)propyl]pyrrolidin-2-one
収率 88.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H]1CN(c2c(F)cc3c(=O)n(N)c(=O)n(C4CC4)c3c2Cl)C[C@H]1c1ccc(O)cc1
Reaction #10402
3-Amino-7-[trans-3-amino-4-(4-hydroxyphenyl)pyrrolidin-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-1H-quinazoline-2,4-dione hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2ccc3c(c2)CCC3)c2nc(NCCCN3CCCC3=O)ncc2c1=O
Reaction #40618
8-Indan-5-yl-5-oxo-2-[3-(2-oxo-pyrrolidin-1-yl)-propylamino]-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
OCCOCCOCCN1CCCC1
Reaction #62993
N-(hydroxyethoxyethoxyethyl)pyrrolidine
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCN1CCCC1=O)c1ccncc1Nc1ccc(I)cc1F
Reaction #67814
3-[(2-fluoro-4-iodophenyl)amino]-N-[3-(2-oxopyrrolidin-1-yl)propyl]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCN1CCCC1=O)[C@@H]1CCCN1C(=O)OCc1ccccc1
Reaction #93118
(S)-1-benzyloxycarbonyl-N-[3-(2-oxo-pyrrolidinyl)propyl]-2-pyrrolidine carboxamide
収率 29.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCN1CCCC1=O)c1ccncc1Nc1ccc(I)cc1F
Reaction #165979
3-[(2-fluoro-4-iodophenyl)amino]-N-[3-(2-oxopyrrolidin-1-yl)propyl]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(NC(=O)c1cc2cc(F)ccc2[nH]1)C(=O)N1CC2CC1CN2C(=O)c1ccc(-c2ccccc2)cn1
Reaction #177467
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccc3c(c2)OCO3)CCN(C(=O)c2ccc(Cl)c(S(N)(=O)=O)c2)CC1
Reaction #177962
DOI: 10.1039/C8SC04228D
Cc1cc(OCCCN2CCCC2=O)cc(C)c1Br
Reaction #183962
DOI: 10.1039/C8SC04228D
CCOC(=O)C=CN1CCCC1
Reaction #196143
DOI: 10.1039/C8SC04228D
COc1ccccc1OC(=O)c1ncn2c1C1CCCN1C(=O)c1c(Cl)cccc1-2
Reaction #205111
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(S(C)(=O)=O)n(C2CC2)c2c(OC(F)F)c(N3CCNCC3)c(F)cc2c1=O
Reaction #207526
DOI: 10.1039/C8SC04228D
CC(C)c1cc(C#N)cc2nc(-c3ccc(C(=O)NCC4CCN(Cc5ccc(Br)cc5)C4)cc3)oc12
Reaction #208491
DOI: 10.1039/C8SC04228D
CC1=C(C(=O)OCCN2CCCC2=O)C(c2ccc(C#N)cc2)N(CC(=O)OC(C)(C)C)C(=O)N1c1cccc(C(F)(F)F)c1
Reaction #211070
DOI: 10.1039/C8SC04228D
CCCCN1CCCC1CO
Reaction #212267
DOI: 10.1039/C8SC04228D
O=C(Oc1cccc(Cl)c1)c1ncn2c1C1CCCN1C(=O)c1c(Cl)cccc1-2
Reaction #212963
DOI: 10.1039/C8SC04228D
Cl
Reaction #226994
DOI: 10.1039/C8SC04228D
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