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COCC1CCCCN1.Cl

CCOC(=O)C1CC(=O)CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44021
oil
Выход 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44022
mixture
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(COC(=O)N(C)C)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44024
112
Выход 136.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CCC[C@@H](c2ccc(Cl)cc2)N1
Reaction #44641
title compound
Выход 37.8%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1CCC[C@@H](c2ccc(Cl)cc2)N1
Reaction #44642
title compound
Выход 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62455
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62490
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1NCCCC1C.Cl
Reaction #89119
methyl 3-methylpiperidine-2-carboxylate hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1c1nc2ccc(Cl)cc2s1
Reaction #181272
DOI: 10.1039/C8SC04228D
C=CC(=O)N1CCC(Oc2cc3c(Nc4ccc(F)c(Cl)c4F)ncnc3cc2OC)CC1C(=O)O
Reaction #182329
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(N=C2OC(C)C3CCCCN23)c(F)cc1Cl
Reaction #200575
DOI: 10.1039/C8SC04228D
NCC(=O)N1CCCC2(S(=O)(=O)c3ccc(Cl)cc3)c3c(F)ccc(F)c3OCC12
Reaction #203903
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CCC(c2cc(N)n3nccc3n2)CN1C(=O)OC(C)(C)C
Reaction #208953
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(Oc4ccc(Cl)cc4)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #221327
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #226296
DOI: 10.1039/C8SC04228D
COC(=O)CCCN1CCCCC1COc1ccc(Oc2ccc(Cl)cc2)cc1
Reaction #234879
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCCCN1C(=S)Cl
Reaction #241164
DOI: 10.1039/C8SC04228D
COc1cc(C=C2CCC3COCC(c4ccc(Cl)cc4)N3C2=O)ccc1-n1cnc(C)c1
Reaction #269391
DOI: 10.1039/C8SC04228D
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(Cl)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #279070
DOI: 10.1039/C8SC04228D
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