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Aus Fermentationslosungen von Streplomyces bluensis NRRL 2876.
D. J. Mason et al., Antimicrob. Agents Chemother. 1963, 607.
М. E. Bergy et al., Antimicrob. Agents Chemother. 1963,614.
DAS 1 183 631 (Upjohn; Anm. 19.7.1962; USA-Prior. 7.8.1961). Struktur:
B. Bannister, A. D. Argoudelis, J. Am. Chem. Soc. 85,119, 234 (1963). I. J. McGilveray, U. L. Rinehart, J. Am. Chem. Soc. 87,4003 (1965).
USA: Bluensomycin ,,Upjohn“ (Upjohn)
Bolasteron 1605-89-6
17/?-hydroxy-7a,17-dimethylandrost-4-en-3-one
Anabolicum
110 В Bolasteron - Boldenonundecylenat - Bromazepam
“КЗ"0
А|[ОС(СН,);[3
Alummium-tri-
(e/f-butylat
3ft 17/3-Dihydroxy-)7a-methyl - 5-androsten (vgi. Methyttestosteron-Synthese, S. 588)
p-Chinon
1. CH3MgBr/CuCl2 OH ^vjJ-СНз 1 I H 1 /
2. Isomerentrerinung Тй j H
1- Methylmagneskjmbromid/
KupferdD-chlond 0' ' -CH3
Bolasteron
USP 3 341 557 (Upjohn; ert. 12.9.1967; Prior. 5.6.1961, 6.11.1960, 6.6.1958). J. A. Campbell, J. C. Babcock, J. Am. Chem. Soc. 81,4069 (1959).
USA: Myagen® (Upjohn)
Boldenonundecylenat
13103-34-9
846-48-0 Boldenon
Anabolicum
17j3-hydroxyandrosta-l,4-dien-3-one-undecenoate
OH
| Pyfidio)
Boldenon
+ H2C=CH-(CH2)8-COCl
10 - Undecensaurechlorid
0-C0-!CH2}8-CH=CH2
Boldenonundecylenat
Belg-P623 277 (Merck AG; Anm. 5.10.1962; D-Prior. 5.10.1961). Ausgangsverbindung:
Can-P 803 490 (Upjohn; Anm. 1956; USA-Prior. 1955).
GB-P 922525 (Loevens Kemiske Fabrik; Laufzeit ab 6.11.1961; Prior. 9.11.1960). USP 2 837 464 (Schering; ert. 1958; Prior. 1955).
USP 2 875 196 (Olin Mathieson; ert. 1959; Prior. 1956,1955).
Ch. Meystre et al, Helv. Chim. Acta 39, 734 (1956).
D: Vebonol®(Ciba) USA; Parenabo]® (Ciba)
Bromazepam 1812-30-2 Tranquilizer
7-bromo-l,3-dihydro-5-(2-pyridyl)-2H-l,4-benzo-diazepin-2-one
Bromazepam В 111
оС»
6" '
2-(2-Amino-
benzoyU-pyridin
NH-CO-CH3
6
2-(2-Acetamido-
benzoyU-pyridin
Br2/CH3COOH
„XX,,
6
NH-СО-СИз
2-(2-Acetamido-5-brombenzoyl)-pyndin
NH2
6
2-{2-Amino-5-
brombenzoyll-
pyridin
h2N-Ch2-COOC2Hs • HCl/Pyridm ^ Glycirwthylester-
a.
Ы^СНз
2-Picolin
H202/CH3C00H
Cl
S-^СНз
0
2-Picolin-1-oxid
COOC2H5 2' COOCgH;
!. Natnunhyarid 2 Oxalsaure-diethylester
a
CH2-C-COOC2H5 II 0
2-Pyndylbrenztrauben-saureethylester-1 -oxid
1. LiAlHt
2. HCl
Cr03/CH,C00H
Bromazepam
2-Aminomethyt-5-bromindo\-
3- (2-pyridyl) - Oihydrochlorid
DOT 9, 238 (1973); 11, 31 (1975). a USP 3 100770 (Roche; ert. 13.8.1963; Anm. 11.8.1961).
USP 3 182 065 (Roche; ert. 4.5.1965; Anm. 9.4.1964; Prior. 19.4.1963).
USP 3 182 066 (Roche; ert. 4.5.1965; Anm. 9.4.1964; Prior. 19.4.1963).
USP 3 182 067 (Roche; ert. 4.5.1965; Anm. 9.4.1964).
R. I. Fryer et al., 1. Pharm. Sri. 53, 264 (1964).
Modifizierte Verfahren:
DAS 2 233 483 (Roche; Anm. 7.7.1972; GB-Prior. 8.7.1971, 7.10.1971).
DOS 2 252 378 (Roche; Anm. 25.10.1972; CH-Prior. 18.11.1971).
Alternativsynthese fur 2-(2-Ammo-5-brombenzoyl)-pyridin:
DAS 2 256 614 (Roche; Anm. 17.11.1972). b DAS 1 813 241 (Roche; Anm. 6.12.1968; J-Prior. 8.12.1967, 9.12.1967, 12.12.1967, 25.4.1968).
112 В Bromazepam - Bromazin - Bromelain
D: Lexotanil® (Roche) I: Lexotan® (Roche)
J: Lexotan® (Nippon Roche) USA: Lectopam® (Roche)
Bromazin
(Bromdiphenhydramin)
118-23-0
1808-12-4 Hydrochlorid
Antihistaminicum
2-(p-brorno-c'-phenylbenzyloxy)-/V,jV-dimethylethylamine
Br
Br
} %
CH-OH
\J
4-Brom-
benzhydrol
PBr3
iccul
Phosphor-
{lll)-bromid
§
Ch
6
4-Brombenz-
hydrylbromid
HO-CH2-CH2-N(CH3)j
2-Dimethylaminoethanol
d
ch-o-ch2-ch2-n
CH3
GB-P 670622 (Parke Davis; Anm. 1948; CH-Prior. 1947).
D: Ambodryl® (Parke-Davis) F; Ambodryl® (Parke-Davis)
I: Ambodryl® (Parke Davis) USA: AmbodryJ® (Parke-Davis)
Bromelain
(Bromelin)
9001-00-7
Antiphlogisticum;
Cytostaticum
a concentrate of proteolytic enzymes derived from Ananas comosus Merr. Proteolytisches Enzym (Glycoprotein) relative Molekiilmasse ~ 33 000
Durch Extraktion aus Ananasstengeln mit Wasser und Fallung mit Aceton oder Ammoniumsulfat. R. M. Heinicke, Science 118,753 (1953).
USP 3 002 891 (Pineapple Research Inst. Hawai; ert. 3.10.1961; Anm. 12.12.1958).
Reinigung:
USP 2 950 227 (Schering AG; ert. 1960; Prior. 1956, 1959).
D: Bromelain 200 (Nadrol)
Mexase® (Ciba)-Komb. traumanase® (Arznei Miiller-Rorer) F: Extranase (Rorer)
Mexase® (Ciba-Geigy)-Komb.
GB: Ananase® (Pharmax)
I: Ananase® (Rorer)
Proteolis® (Benvegna)
Rogorin® (Saba)
Komb, Prap.
J: Ananase® (Yamanouchi)
Bromelain (Iwaki; Jintan; Nakano; Nippon Kayaku; Sawai)
Bromelin (Green Cross; Sankyo) Pinase® (Dainippon)
USA; Ananase® (Rorer)
Bromhexin - Bromindion В 113
Bromhexin 3572-43-8 Broncho-Secretolyticum
611 -75-6 Hydrochlorid
3,5-dibrorno-;V“-cyc]ohexyl-/Vr'-methyltoluene-a-2-diamine
CH3
/
CH2-B' / 3 r^VCH2_N4 H;N —NH2 /Raney-Ni '
», •"k ~ ~—
О
2-NitrO' Cyclohexyl-
benzylbromid methylamin
N-\2-Aminobenzyl)- j Bromhexin
W-cyclohexyl-W-
methylamin
DBP 1 169939 (Thomae; Anm. 20.11.1961).
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