NZ245662A - Quinazoline derivatives, preparation and pharmaceutical compositions thereof - Google Patents

Info

Publication number

NZ245662A

NZ245662A NZ245662A NZ24566293A NZ245662A NZ 245662 A NZ245662 A NZ 245662A NZ 245662 A NZ245662 A NZ 245662A NZ 24566293 A NZ24566293 A NZ 24566293A NZ 245662 A NZ245662 A NZ 245662A

Authority

NZ

New Zealand

Prior art keywords

alkyl

alkoxy

amino

alkylamino

quinazoline

Prior art date

1992-01-20

Links

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• Global Dossier
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• 238000002360 preparation method Methods 0.000 title claims abstract description 16
• 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 7
• 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 title abstract description 5
• -1 hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 claims abstract description 338
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 267
• 125000003545 alkoxy group Chemical group 0.000 claims abstract description 150
• 150000001875 compounds Chemical class 0.000 claims abstract description 93
• 238000000034 method Methods 0.000 claims abstract description 63
• 150000003839 salts Chemical class 0.000 claims abstract description 55
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 34
• 239000001257 hydrogen Substances 0.000 claims abstract description 26
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 26
• 125000005843 halogen group Chemical group 0.000 claims abstract description 25
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 23
• 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 21
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 15
• 125000005530 alkylenedioxy group Chemical group 0.000 claims abstract description 14
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 13
• 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 9
• 230000008569 process Effects 0.000 claims abstract description 9
• 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims abstract description 7
• 125000005115 alkyl carbamoyl group Chemical group 0.000 claims abstract description 6
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 5
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 5
• 125000000033 alkoxyamino group Chemical group 0.000 claims abstract description 4
• 125000002349 hydroxyamino group Chemical group [H]ON([H])[*] 0.000 claims abstract description 4
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 5
• 125000003282 alkyl amino group Chemical group 0.000 claims description 102
• 150000003246 quinazolines Chemical class 0.000 claims description 85
• 125000005236 alkanoylamino group Chemical group 0.000 claims description 80
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 36
• QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims description 28
• 238000004519 manufacturing process Methods 0.000 claims description 24
• 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 22
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 18
• 125000004414 alkyl thio group Chemical group 0.000 claims description 18
• 238000006243 chemical reaction Methods 0.000 claims description 18
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 16
• 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 15
• JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims description 14
• VKOGLNSKGDTRGH-UHFFFAOYSA-N 4-[(6-methoxyquinazolin-4-yl)amino]phenol Chemical compound C12=CC(OC)=CC=C2N=CN=C1NC1=CC=C(O)C=C1 VKOGLNSKGDTRGH-UHFFFAOYSA-N 0.000 claims description 13
• GBJXFMREUNFKRX-UHFFFAOYSA-N 4-n-(4-aminophenyl)quinazoline-4,6-diamine Chemical compound C1=CC(N)=CC=C1NC1=NC=NC2=CC=C(N)C=C12 GBJXFMREUNFKRX-UHFFFAOYSA-N 0.000 claims description 13
• JFDWMFYUKLPRSP-UHFFFAOYSA-N 6-methyl-n-phenylquinazolin-4-amine Chemical compound C12=CC(C)=CC=C2N=CN=C1NC1=CC=CC=C1 JFDWMFYUKLPRSP-UHFFFAOYSA-N 0.000 claims description 13
• 230000001093 anti-cancer Effects 0.000 claims description 13
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 13
• CRZPVSMPJCPEPP-UHFFFAOYSA-N 4-([1,3]dioxolo[4,5-g]quinazolin-8-ylamino)phenol Chemical compound C1=CC(O)=CC=C1NC(C1=C2)=NC=NC1=CC1=C2OCO1 CRZPVSMPJCPEPP-UHFFFAOYSA-N 0.000 claims description 12
• MJKCGAHOCZLYDG-UHFFFAOYSA-N 6,7-dimethoxy-n-phenylquinazolin-4-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=NC=1NC1=CC=CC=C1 MJKCGAHOCZLYDG-UHFFFAOYSA-N 0.000 claims description 12
• 241001465754 Metazoa Species 0.000 claims description 12
• 239000000126 substance Substances 0.000 claims description 12
• 125000001424 substituent group Chemical group 0.000 claims description 12
• YPBYGBLLRMWZAF-UHFFFAOYSA-N 4-[(6,7,8-trimethoxyquinazolin-4-yl)amino]phenol Chemical compound N1=CN=C2C(OC)=C(OC)C(OC)=CC2=C1NC1=CC=C(O)C=C1 YPBYGBLLRMWZAF-UHFFFAOYSA-N 0.000 claims description 11
• 125000004423 acyloxy group Chemical group 0.000 claims description 10
• BYBQXGBBLHNCIR-UHFFFAOYSA-N 4-(4-chloroanilino)quinazolin-8-ol Chemical compound N1=CN=C2C(O)=CC=CC2=C1NC1=CC=C(Cl)C=C1 BYBQXGBBLHNCIR-UHFFFAOYSA-N 0.000 claims description 8
• ZFSSJGZFLIOOKN-UHFFFAOYSA-N 4-(4-methoxyanilino)quinazolin-8-ol Chemical compound C1=CC(OC)=CC=C1NC1=NC=NC2=C(O)C=CC=C12 ZFSSJGZFLIOOKN-UHFFFAOYSA-N 0.000 claims description 8
• URJYCHBAPFKHRE-UHFFFAOYSA-N 8-methoxy-n-(4-methoxyphenyl)quinazolin-4-amine Chemical compound C1=CC(OC)=CC=C1NC1=NC=NC2=C(OC)C=CC=C12 URJYCHBAPFKHRE-UHFFFAOYSA-N 0.000 claims description 7
• 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 7
• 239000003795 chemical substances by application Substances 0.000 claims description 7
• MPIHIJBPYYKLEA-UHFFFAOYSA-N n-(4-chlorophenyl)-8-methoxyquinazolin-4-amine Chemical compound N1=CN=C2C(OC)=CC=CC2=C1NC1=CC=C(Cl)C=C1 MPIHIJBPYYKLEA-UHFFFAOYSA-N 0.000 claims description 7
• 239000002253 acid Substances 0.000 claims description 6
• 125000001246 bromo group Chemical group Br* 0.000 claims description 6
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
• 125000001153 fluoro group Chemical group F* 0.000 claims description 6
• 230000003647 oxidation Effects 0.000 claims description 6
• 238000007254 oxidation reaction Methods 0.000 claims description 6
• 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 5
• 230000009467 reduction Effects 0.000 claims description 5
• 230000010933 acylation Effects 0.000 claims description 4
• 238000005917 acylation reaction Methods 0.000 claims description 4
• 230000029936 alkylation Effects 0.000 claims description 4
• 238000005804 alkylation reaction Methods 0.000 claims description 4
• 125000001589 carboacyl group Chemical group 0.000 claims description 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
• 238000003776 cleavage reaction Methods 0.000 claims description 4
• 239000003085 diluting agent Substances 0.000 claims description 4
• 239000003814 drug Substances 0.000 claims description 4
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
• BCZUPYLJRTXVOY-UHFFFAOYSA-N 6,7-diethoxy-n-(3-methylphenyl)quinazolin-4-amine Chemical compound C=12C=C(OCC)C(OCC)=CC2=NC=NC=1NC1=CC=CC(C)=C1 BCZUPYLJRTXVOY-UHFFFAOYSA-N 0.000 claims description 3
• YMQNMNWEDFTMTJ-UHFFFAOYSA-N 6-n,6-n-dimethyl-4-n-(3-methylphenyl)quinazoline-4,6-diamine Chemical compound C12=CC(N(C)C)=CC=C2N=CN=C1NC1=CC=CC(C)=C1 YMQNMNWEDFTMTJ-UHFFFAOYSA-N 0.000 claims description 3
• BWENYVDMLAZGTP-UHFFFAOYSA-N 7-methoxy-4-n-(3-methylphenyl)quinazoline-4,6-diamine Chemical compound C=12C=C(N)C(OC)=CC2=NC=NC=1NC1=CC=CC(C)=C1 BWENYVDMLAZGTP-UHFFFAOYSA-N 0.000 claims description 3
• WLGDTJBSQGRVRX-UHFFFAOYSA-N [4-(3-methylanilino)quinazolin-6-yl]urea Chemical compound CC1=CC=CC(NC=2C3=CC(NC(N)=O)=CC=C3N=CN=2)=C1 WLGDTJBSQGRVRX-UHFFFAOYSA-N 0.000 claims description 3
• 150000001412 amines Chemical class 0.000 claims description 3
• 230000007062 hydrolysis Effects 0.000 claims description 3
• 238000006460 hydrolysis reaction Methods 0.000 claims description 3
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 3
• 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 3
• BIGXXKQBMRKUJG-UHFFFAOYSA-N n-(3-methylphenyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-amine Chemical compound CC1=CC=CC(NC=2C3=CC=4OCCOC=4C=C3N=CN=2)=C1 BIGXXKQBMRKUJG-UHFFFAOYSA-N 0.000 claims description 3
• VQIWZLBIZSXBLT-UHFFFAOYSA-N n-[4-(3-methylanilino)quinazolin-6-yl]benzamide Chemical compound CC1=CC=CC(NC=2C3=CC(NC(=O)C=4C=CC=CC=4)=CC=C3N=CN=2)=C1 VQIWZLBIZSXBLT-UHFFFAOYSA-N 0.000 claims description 3
• QYXLGBIMSTYMHA-UHFFFAOYSA-N 6,7-dimethoxy-n-(3-nitrophenyl)quinazolin-4-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=NC=1NC1=CC=CC([N+]([O-])=O)=C1 QYXLGBIMSTYMHA-UHFFFAOYSA-N 0.000 claims description 2
• ULUILBSHRZPHGK-UHFFFAOYSA-N 6-(2-methoxyethoxymethyl)-n-(3-methylphenyl)quinazolin-4-amine Chemical compound C12=CC(COCCOC)=CC=C2N=CN=C1NC1=CC=CC(C)=C1 ULUILBSHRZPHGK-UHFFFAOYSA-N 0.000 claims description 2
• ZJCCYDYNZMGIHC-UHFFFAOYSA-N 6-methoxy-n-(3-methylphenyl)quinazolin-4-amine Chemical compound C12=CC(OC)=CC=C2N=CN=C1NC1=CC=CC(C)=C1 ZJCCYDYNZMGIHC-UHFFFAOYSA-N 0.000 claims description 2
• XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 2
• 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 2
• 125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims description 2
• NZHRGFLNIISRAV-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-6,7-dimethoxyquinazolin-4-amine Chemical compound C=12C=C(OC)C(OC)=CC2=NC=NC=1NC1=CC=C(Cl)C(Cl)=C1 NZHRGFLNIISRAV-UHFFFAOYSA-N 0.000 claims description 2
• JDEKFVYZUIPHET-UHFFFAOYSA-N n-(3-chlorophenyl)-6-methoxyquinazolin-4-amine Chemical compound C12=CC(OC)=CC=C2N=CN=C1NC1=CC=CC(Cl)=C1 JDEKFVYZUIPHET-UHFFFAOYSA-N 0.000 claims description 2
• 230000007017 scission Effects 0.000 claims description 2
• ACCVTKJXKFSAAH-UHFFFAOYSA-N 5-methoxyquinazoline Chemical compound C1=NC=C2C(OC)=CC=CC2=N1 ACCVTKJXKFSAAH-UHFFFAOYSA-N 0.000 claims 1
• MCBABIOGLXZCHP-UHFFFAOYSA-N 6,7-dimethoxy-n-phenylquinazolin-2-amine Chemical compound N1=C2C=C(OC)C(OC)=CC2=CN=C1NC1=CC=CC=C1 MCBABIOGLXZCHP-UHFFFAOYSA-N 0.000 claims 1
• UWSJFQYJMQTBQA-UHFFFAOYSA-N 6-methyl-N-phenylquinazolin-2-amine Chemical compound N1=CC2=CC(C)=CC=C2N=C1NC1=CC=CC=C1 UWSJFQYJMQTBQA-UHFFFAOYSA-N 0.000 claims 1
• 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
• 206010028980 Neoplasm Diseases 0.000 abstract description 17
• 102000027426 receptor tyrosine kinases Human genes 0.000 abstract description 16
• 108091008598 receptor tyrosine kinases Proteins 0.000 abstract description 16
• 238000011282 treatment Methods 0.000 abstract description 13
• 201000011510 cancer Diseases 0.000 abstract description 9
• 230000002401 inhibitory effect Effects 0.000 abstract description 8
• 239000000203 mixture Substances 0.000 description 299
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 201
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 138
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 114
• 238000000921 elemental analysis Methods 0.000 description 85
• 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 84
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 68
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 59
• 239000000243 solution Substances 0.000 description 57
• 238000004440 column chromatography Methods 0.000 description 56
• 239000003480 eluent Substances 0.000 description 56
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 49
• 239000007858 starting material Substances 0.000 description 44
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 43
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 39
• 238000010992 reflux Methods 0.000 description 36
• 239000000047 product Substances 0.000 description 32
• 238000012360 testing method Methods 0.000 description 32
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 27
• DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 26
• 239000002244 precipitate Substances 0.000 description 26
• FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 25
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 22
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 21
• JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 20
• 239000012074 organic phase Substances 0.000 description 20
• 239000012258 stirred mixture Substances 0.000 description 20
• WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 18
• ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 18
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
• 239000000463 material Substances 0.000 description 18
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
• 210000004027 cell Anatomy 0.000 description 16
• 239000011541 reaction mixture Substances 0.000 description 16
• 239000007787 solid Substances 0.000 description 16
• NFBCSWGEYDCCDW-UHFFFAOYSA-N 4-n-(3-methylphenyl)quinazoline-4,6-diamine Chemical compound CC1=CC=CC(NC=2C3=CC(N)=CC=C3N=CN=2)=C1 NFBCSWGEYDCCDW-UHFFFAOYSA-N 0.000 description 15
• 241000282414 Homo sapiens Species 0.000 description 13
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 12
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• XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 12
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 12
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
• 229910000027 potassium carbonate Inorganic materials 0.000 description 11
• ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 10
• 125000004356 hydroxy functional group Chemical group O* 0.000 description 10
• 239000012071 phase Substances 0.000 description 10
• CMYBAHRLNADCKS-UHFFFAOYSA-N 6-(bromomethyl)-n-(3-methylphenyl)quinazolin-4-amine Chemical compound CC1=CC=CC(NC=2C3=CC(CBr)=CC=C3N=CN=2)=C1 CMYBAHRLNADCKS-UHFFFAOYSA-N 0.000 description 9
• 239000002585 base Substances 0.000 description 9
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• 239000003921 oil Substances 0.000 description 9
• LLLHRNQLGUOJHP-UHFFFAOYSA-N 4-chloro-6,7-dimethoxyquinazoline Chemical compound C1=NC(Cl)=C2C=C(OC)C(OC)=CC2=N1 LLLHRNQLGUOJHP-UHFFFAOYSA-N 0.000 description 8
• KPHNOFBKQHPSGB-UHFFFAOYSA-N 6-methoxy-4-(3-methylanilino)quinazolin-7-ol Chemical compound N1=CN=C2C=C(O)C(OC)=CC2=C1NC1=CC=CC(C)=C1 KPHNOFBKQHPSGB-UHFFFAOYSA-N 0.000 description 8
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• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
• 239000012458 free base Substances 0.000 description 8
• HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 8
• 239000012044 organic layer Substances 0.000 description 8
• 230000002829 reductive effect Effects 0.000 description 8
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• 102400001368 Epidermal growth factor Human genes 0.000 description 7
• 101800003838 Epidermal growth factor Proteins 0.000 description 7
• 229960000583 acetic acid Drugs 0.000 description 7
• 239000003054 catalyst Substances 0.000 description 7
• 229940116977 epidermal growth factor Drugs 0.000 description 7
• 230000012010 growth Effects 0.000 description 7
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