子结构搜索

CN(C)CCO

COc1nc(Nc2ccc3c(n2)OC(c2cc(C)ccn2)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #486
收率 43.1%
COc1nc(Nc2ccc3c(n2)OC(c2ccc(C)cn2)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #487
收率 67.7%
CC(=NOCCN1CCOCC1)c1ccccc1
Reaction #10272
acetophenone O-[2-((morpholin-4-yl))ethyl]oxime
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1NC(=O)CCC(=O)O
Reaction #11771
title compound
收率 31.2%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CN2CCOCC2)c2cccnc12
Reaction #52217
title product
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=O)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52655
3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde
收率 14.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Cl)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52656
5-chloro-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
收率 10.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Br)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52688
5-bromo-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
收率 13.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63654
methoxy acetyl carnitine chloride
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63655
title compound
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CNCCN1CCc1ccc2c(c1)OCCO2
Reaction #67962
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(CCn2c(=O)cc(C)c3ccc(OC)cc32)CCN1CCc1ccc2c(c1)OCCO2
Reaction #68084
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)-4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-2-carboxylate
收率 64.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71792
title compound
收率 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1csc(N2CC[C@H](N)[C@H](OC)C2)n1
Reaction #71793
Ethyl cis(±)-[2-(4-amino-3-methoxypiperidin-1-yl)-1,3-thiazol-4-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)sc1C
Reaction #72093
title compound
收率 7.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #76781
tan crystalline subtitle compound
收率 48.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #77878
tan crystalline subtitle compound
收率 48.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2C(=O)CC[C@H]2C(=O)O)cc1
Reaction #83395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
收率 99.1%DOI: 10.6084/m9.figshare.5104873.v1
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