部分構造検索

NCCN1CCOCC1

C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N)C1=O
Reaction #7387
title compound
収率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)c2cc3cc(Cl)ccc3o2)C1=O
Reaction #7416
title compound
収率 55.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(-c2ccc(F)cc2)c(-c2ccnc(Oc3ccccc3)n2)n2n1CC(N1CCOCC1)C2
Reaction #7744
desired product
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(CCOc2ccc(Cc3ccc(-c4ncco4)cc3)cc2)CCN2CCOCC2)cc1
Reaction #44810
methyl 4-[[[2-(4-morpholinyl)ethyl][2-[4-[[4-(2-oxazolyl)phenyl]methyl]phenoxy]ethyl]amino]-methyl]benzoate
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CN(CCOc2ccc(Cc3ccc(-c4ncco4)cc3)cc2)CCN2CCOCC2)cc1
Reaction #44811
4-[[[2-(4-morpholinyl)ethyl][2-[4-[[4-(2-oxazolyl)phenyl]methyl]phenoxy]ethyl]-amino]methyl]benzoic acid
収率 5.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(-c2ccc(F)cc2)c(-c2ccnc(Oc3ccccc3)n2)n2n1CC(N1CCOCC1)C2
Reaction #50952
desired product
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)CC(N4CCOCC4)C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60076
1-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]-ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]-3-morpholin-4-ylpyrrolidine-2,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCN(CCN2CCOCC2)S(=O)(=O)c2ccccc2[N+](=O)[O-])nc1
Reaction #60214
(2-morpholin-4-ylethyl){2-[(5-nitro(2-pyridyl))amino]ethyl}[(2-nitrophenyl)sulfonyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N)C1=O
Reaction #61706
title compound
収率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)c2cc3cc(Cl)ccc3o2)C1=O
Reaction #61716
title compound
収率 55.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3cccc(C(=O)NCCN4CCOCC4)c3cn2)cn1
Reaction #68963
title compound
収率 32.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(C3CCN(CCN4CCOCC4)CC3)noc2c1
Reaction #83915
N-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]morpholine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c(N)c1-c1nc2ccc(S(=O)(=O)NCCN3CCOCC3)cc2s1
Reaction #85535
title compound
収率 44.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](Cc1ccccc1)C(=O)[C@@]1(C)CO1
Reaction #87187
(S)-3-cyclopropyl-N-((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-yl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanamide
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sccc1S(=O)(=O)N(C)CCN1CCOCC1
Reaction #88021
methyl 3-(N-methyl-N-(2-morpholinoethyl)sulfamoyl)thiophene-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCN1CCOCC1)S(=O)(=O)c1ccsc1C(=O)O
Reaction #88022
3-(N-methyl-N-(2-morpholinoethyl)-sulfamoyl)thiophene-2-carboxylic acid
収率 83.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(CCN3CCOCC3)c12
Reaction #155337
5-fluoro-3-(4-methoxyphenyl)-1-(2-morpholin-4-ylethyl)-8-propoxy-1H-quinolin-4-one
収率 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(F)c2c(=O)c(-c3ccc(O)cc3)cn(CC(=O)NCCN3CCOCC3)c12
Reaction #155346
2-[5-fluoro-3-(4-hydroxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]-N-(2-morpholin-4-ylethyl)acetamide
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN(CC(=O)N1CCOCC1)C(=O)CBr
Reaction #174504
DOI: 10.1039/C8SC04228D
O=C1CCC(C(=O)N2CCN(CC(=O)N3CCOCC3)CC2)N1
Reaction #183553
DOI: 10.1039/C8SC04228D
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