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. .: , 2007. 608 c.
ISBN 5-98657-009-
( ): pharmazeutischewirkstoffe1982.djvu
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DBP 1 179 943 (Thomae; Anm. 8.11.1962).
Kombination mit Antiphlogistica:
DOS 2 708 520 (Thomae; Anm. 26.2.1977).
USP 4154833 (Boehringer Ing.; ert. 15.5.1979; D-Prior. 26.2.1977).
D: Gastrozepin® (Thomae)
Gastrozepin (Boehringer Ing.)
Pirenzepin - Piribedil - Piritramid - Piromidinsaure P 739
Piribedil 3605-01-4 Vasodilatator
52293-23-9 Methansulfonat
2-(4-piperonyl-l-piperazinyl)pyrimidine
N)-CI + HN VcH2-^°
2-Chlor- 1-{3/-Methylendioxy-pyrimidin benzyl)-piperazin
DOT 6,29(1970).
USP 3 299 067 (Science Union; ert, 17.1.1967; GB-Prior. 19.11.1963).
GB-P 1 101425 (Science Union; Anm. 19.11.1963; Laufzeit ab 18.11.1964). G. J. Regnier et al., J. Med Chem. 11,1151 (1968).
D: Trivastal®(Pharmacodex) I; Trivastan® (Servier)
F: Trivastal® (Eutherapie)
pjritramid 302-41-O Analgeticum
(Pirinitramid)
r-(3-cyano-3,3-diphehylpropyl)-(l,4’-bi pi-peridine)-4’-carboxamide or l-(3-cyano-3,3-diphenylpropyl)-4-piperidino-piperidine-4-carboxylic acid amide
P
c-c-c
6
/—\ ,co-nh2
NC-C-CH2-CH2-8r + HN^_
О
3,3-Dipheny I-3-cyan-propytbromid
4-Pipendinopipendin-4-carboxamid ti-Carbamoyl-4-piperidinopiperidin)
(vgl. Pipamparon-Synthese, S. 729)
,C0-NH2
Q
T C(
C-C-CH2-CH2-N X
6 О
DOT 5,106(1969).
DBP 1238 472 (Janssen; Anm. 2.8.1961; USA-Prior. 3.8.1960).
D: Dipidolor*® (Janssen)
GB: Dipidolor^ (Janssen)
Piromidinsaure
(Piromidic acid)
19562-30-2
Chemotherapeuticum (gegen gramnegative Bakterien)
8-ethyl-5,8-dihydro-5-oxo-2-(l-pyrrolidinyl)pyrido[2,3-<i]-pyrimidine-6-carboxylic acid
740 P Piromidinsaure - Piroxicam
HOOC'
C2H5
jQC
S —CH3 HN^j /C2HsOH ; 95°C
3-Ethyl-2-methy(thio-5-oxo-5,B-dihydro-pyrido{2,3-d]-pyrimidin-6-carbonsaure (vgl. PipemnHnsdure-Synthese. S. 731)
C2H5 ^
HO0C^|x^xN
0
Piromfdinsaure
DOS 2 143 369 (Dainippon; Anm. 30.8.1971; J-Prior. 29.8.1970).
USP 3 673 184 (Dainippon; ert. 27.6.1972; Prior. 8.9.1966, 2.9.1970).
GB-P 1 129 358 (Dainippon; Anm. 8.9.1966; J-Prior. 8.9.1965,10.8.1965). Alternativ-Verfahren :
DOS 2 338 325 (Roger Bellon; Anm. 1.8.1973; F-Prior. 2.8.1972).
USP 4 125 720 (Roger Bellon; ert. 14.11.1978; F-Prior. 16.4.1976).
D: Septural® (Gruenenthal) 1: Pirodal® (Isf)
F; Bactamyl® (Carrion) J: Panacid® (Dainippon)
PirOXiCam 36322-90-4 Antiphlogisticum
4-hydroxy-2-methyl-/V-2-pyridyl-2H-l,2-benzothiazine-3-carboxamide 1,1-dioxide
Saccharin
(Natrium-Salz)
Cl—CH;—COOCH3 CMoressigsaure-methyteslef
CH^l/NaOH
-CH2-COOCH3
0
СООСНЗ
2-AmiPto pyr idin
£
NH
‘СООСНз 0
3-Methoxycarbonyl -4 -oxo-3,4-dihydro-2W-1,2-benzothiazin-IJ-dioxid
DOF 2, 125 (1977).
USP 3 591584 (Pfizer; ert. 6.7.1971; Anm. 27.8.1968).
DOS 1 943 265 (Pfizer; Anm. 26.8.1969; USA-Prior. 27.8.1968). Altemativ-Syn these;
USP 3 892 740 (Pfizer; ert. 1.7.1975; Anm. 15.10.1974).
D: Felden® (Mack/Pfizer)
GB: Feldene® (Pfizer)
Pivampicillin - Pivmecillinam P 741
Pivampicillin 33817-20-8 Antibioticum
26309-95-5 Hydrochlorid
D-(-)-(a-aminobenzyJ)penicillin hydroxymethyl ester, pivalate (ester) orD-(-)-6-(2-amino-2-phenyl-acetamido)-3,3-dimethyl-7-oxo-4-thia-l-azabicyclo[3.2.0]-heptane-2-carboxylicacid hydroxymethyl ester, pivalate (ester)
^VcH-CO-NH-i—р5уСН3 + С1-СН2-0-С0-С(СНз)з —
N3 /-"A,
fcOOK
Azidocillin Pivalinsaure-chlormethylester
(Kalium-Salz)
(s. s. 68)
H H
L VcH-C0-NH4—f'SvCH’
0ДЛнз
C0-0-CH2-0-C0-C(CH3)3
H2/Pd-C
(Q^CH-CO-NH-i-f-S <
NH, /N'/l
H H
.CH3
NH2 СГ n4 ch3
C0-0-CH2~0-C0-C(CH3|3
Pivampicillin
DOT 7,183 (1971); 8, 148 (1972).
USP 3 697 507 (Lovens Kem. Fabr.; ert. 10.10.1972; Anm. 26.9.1968; GB-Prior. 29.9.1967).
GB-P 1 215 812 (Lovens Kem. Fabr.; Anm. 29.9.1967; Laufzeit ab 27.9.1968).
DAS 1 795 702 (Loevens; Anm. 27.9.1968; GB-Prior. 10.11.1967, 3.1.1968, 22.3.1968).
DAS 1 795 713 (Loevens; Anm. 27.9.1968; GB-Prior. 29.9.1967, 5.10.1967, 23.10.1967,10.11.1967, 6.12.1967,3.1.1968,22.3.1968).
Kristalline Form:
USP 3 956 279 (Leo; ert. 11.5.1976; Anm. 21.9.1973).
DAS 2 349 971 (Leo; Anm. 4.10.1973; GB-Prior. 6.10.1972).
D: Berocillin® (Thomae) F: Pivatil® (Chibret)
Maxifen® (Sharp & Dohme/Boehringer Mannh.) Pondocil (Leo)
Uro Berocillin® (Thomae)-Komb. I: Pondocillina® (Sigmatau)
Pivmecillinam 32886-97-8 Antibioticum
hydroxymethyl(2S,5/?,6/?)-6-[[(hexahydro-lH-azepin-l-yl)methylene]-amino]-3,3-dimethyl-7-oxo-4-thia-l-azabicyclo[3.2.0]heptane-2-carboxylate pivalate (ester)
н
/-Й-Лн, * ^ 0±Хднз
COONa ^c'-0-CH2-0-Cx
6-Aminopenicilian- Pivalinsaurechlormethylester 6-Aminopenicillansaure-pivaloyloxy-
saure methylester (als Tosytat)
742 P Pivmecillinam - Pizotifen
1. NaHC03
2. СНОэ ! NIC2H5 )3
о-
COCl
•СНО/1 / (СаН5)гОа -20®1 С0С1
3. W-Formylhexamethylenimin /
Г N-CH=N-
-Sx CH3
СНз
>^о-сн2-о-сч o' N\
Pivmecillinam
С(СНз)з
DOS 2 055 531 (Loevens; Anm. 11.11.1970; GB-Prior. 11.11.1969,8.7.1970). GB-P 1 293 590 (Loevens; Anm. 11.11.1969, 8.7.1970; Laufzeit ab 10.11.1970). USP 3 957 764 (Loevens; ert. 18.5.1976; GB-Prior. 11.11.1969, 8.7.1970). Kombination mit Trimethoprim:
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