Substructure Search

N

CCOC(=O)c1nc(C(=O)OC(C)(C)C)c[nH]1
Reaction #1702
tert-butyl 2-ethoxycarbonylimidazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nccn1Cc1c(F)cccc1Cl
Reaction #6579
2-n-butyl-1-(2-chloro-6-fluorophenyl)methyl-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(Cc1ccc(O)cc1)C(=O)NC(Cc1ccc(F)cc1)C(=O)N1CC(Cc2ccc3ccccc3c2)NC(=O)C1Cc1c[nH]cn1
Reaction #8632
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81168
title compound
Yield 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81170
title compound
Yield 79.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #81242
title compound
Yield 95.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81244
title compound
Yield 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81268
title compound
Yield 76.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81273
title compound
Yield 98.4%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc(C(C)(C)O)c(C(=O)OC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81282
title compound
Yield 93.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #81283
title compound
Yield 98.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(C(C)OC)[nH]c1C(=O)OC
Reaction #81334
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3n2C(C)C)CC1
Reaction #190962
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
COC(=O)C(C)Oc1cccnc1Oc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)c(F)cc1Cl
Reaction #195098
DOI: 10.1039/C8SC04228D
CCOCCn1c(NC2CCN(CCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #196540
DOI: 10.1039/C8SC04228D
CCN(C(=O)c1cccc(Oc2cc(C(C)(O)c3cncn3C)ccc2C#N)c1)c1ccccc1
Reaction #197581
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3[nH]2)CC1
Reaction #199979
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
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