3- Propylamino

Dihydro-2-(2-methoxy)ethyl-4-propylamino-2H-thieno[3,2-e]-l,2-thiazine-6-sulfonamide-l,1-dioxide hydrochloride was obtained by the reaction of 3,4-dihydro-4-hydroxy-2-(2-methoxy)ethyl-2H-thieno[3,2-e]-l,2-thiazine-6-sulfonamide-1,1-dioxide in THF containing triethylamine with tosyl chloride at -16°C and the next stirring for 18 hrs at room temperature. After which time the mixture was cooled to 0°C and propylamine was added, the desired product (0.57 g, 46%) was obtained m.p. 178°-181°C. [Pg.667]

Amino-4-propylamino-benzol- XII/1, 378 Amino-(2-thienyl)-methan- E2, 313... [Pg.1027]

Nitro-l-propen- -dimethylester E2, 371 3-Nltro-4-propylamino-benzol- XII/1, 378, 379 Octadecan- -bis-[bis-(2-hydrocy-ethyl)-amid] XII/1, 536... [Pg.1040]

Hepten 3-Methyl-4-propylamino-E21b, 1896 (H3C-CH = CH-CH2-M + H7C3-CH = N-C3H7)... [Pg.945]

Pyrimido[4,5-d]pyridazin 5-Amino-8-hydroxy-4-propylamino-2-pyr-rolidino- E9c, 354 (Imino —N-lnsertion)... [Pg.1177]

Methyl l-propyl-4-(propylamino)-2,6-di-m-tolyl-1,2,5,6-tetrahydropyridme-3-carboxylate (4d) White crystals, mp 151-153 °C reaction time 40 h yield 53%... [Pg.96]

Anuno-4-hydroxy-3-propylphenyl)ethanone, 893 1 -(3-Amino-2-hydroxy-5-propylphenyl)ethanone, 893 1 -(4-Amino-2-hydroxy-3-propyIphenyOethanone, 893 1 -[2-(Dimethylamino)-6-hydroxy-4-metliylphenyl]ethanone, 894 1 -[2-Hydroxy-4-(propylamino)phenyl]e(hanone, 894... [Pg.2515]

PYRROLEANDPYRROLEDERIVATIVES] (Vol20) (+)-N-(2-Hydroxy-3-[ql(4-hydroxyphenoxy)propylamino)ethyl morphine-4-caiboxamide... [Pg.502]

The use of selective P-antagonists for treatment of CHF has included the P -blocker metoprolol (Table 1) and results of clinical trials suggest long-term beneficial effects. Selective P -antagonists have also been tested, an example of which is xamoterol [81801 -12-9], C2 H25N20, which is (i)-A/-(2-hydroxy-3-(4-hydroxyphenoxy)propylamino)ethylmorphine-4-carboxamide. Xamoterol exhibits approximately 50% of the activity of isoproterenol, and serves to provide modest inotropic effects (128,129). [Pg.129]

IQ was derived using propylenediamine to the appropriate propylamino derivative and acylated with 4-nitrobenzoyl chloride to nitrobenzamides 105 the ni-trobenzamides were used as haptens to generate the anti-IQ specific monoclonal antibodies (87H2069). [Pg.236]

The lithium salt of 2-(di-wo-propylamino)-l,2-thiaborolide with [( -Cp ) RuC1]4 or [(i -Cp )ZrCl3] yields sandwiches similar to 39 (M = Ru, ZrCl2) (OOOM4935). The same anionic ligand enters a sequence of reactions with dimethylchlorosilane, lithium cyclopentadienyl, lithium di-wo-propylamide, and zirconium(IV) chloride to give sandwich 41. [Pg.19]

Reaction of 2-aminopyridine and 6-chloro-1,3-dipropyl-l//,3//-pyrimi-dine-2,4-dione in THE in the presence of NaH at room temperature overnight gave a mixture of 4-[A-(propylaminocarbonyl)-A-propylamino]-2//-pyrido[l,2-n]pyrimidin-2-one (349) and 6-(2-pyridylamine)-l,3-dipropyl-l//,3//-pyrimidine-2,4-dione (350, R = H) (94JHC81). Only the non-cyclized product 350 (R = Cl) was obtained from 5-chloro-2-aminopyridine. [Pg.242]

Chamical Nama 4-Methyl-3-[ [ 1 -oxo-2-(propylamino) propyl] amino]-2-thiophene carboxylic acid methyl ester... [Pg.257]

Chemical Name 4-chloro-N-[(propylamino)carbonyl] benzenesulfonamide Common Name 1-(p-chloroben2enesulfonyl)-3-propylurea Structural Formula ... [Pg.323]

Chemical Name N-(2-methylphenyl)-2-(propylamino)-Propanamide hydrochloride Common Name Propitocaine hydrochloride... [Pg.1294]

Peptide-type models were synthesized by Jones et a/.44, and by Takemoto etal.45). Takemoto and co-workers46 prepared polymers of 6-methylamino-, 6-di-n-propylamino-, and 6-di-n-butylamino-9-vinylpurines. They reported that these models showed no hypochromic effect on RNA in aqueous solution. [Pg.145]

Benzil, 4,4 -bis(di-n-propylamino)-, 41,3 Benzoic acid, conversion to peroxy-benzoic acid, 43, 93 reduction to 1,4-dihydrobenzoic acid, 43, 22... [Pg.107]

In contrast, o-(A-etboxalyl-A(-propylamino)nitrobenzene (63) gave l-bydroxy-4-propyl-2,3(l//,4F/)-quinoxalinedione (65), perhaps via tbe partly reduced substrate (64) [Pd/C, Hj (3 atm), MejNCHO, 3 b 85%) likewise, 1-(etboxalylamino)-3-fluoro-6-nitrobenzene (66) gave 6-fluoro-l-bydroxy-2,3(l//,4fl)-quinoxalinedione (67) (Zn, NH4CI, HaO-MeaNCHO, <35°C, 57%) and tbe 4-bydroxy isomer was made in even better yield using hydro-... [Pg.11]

CN 4-methyl-3-[[l-oxo-2-(propylamino)propyl]amino]-2-thiophenecarboxylic acid methyl ester monohydrochloride... [Pg.361]

CN l-[2-[2-hydroxy-3-(propylamino)propoxy]phenyl]-3-phenyl-l-propanone hydrochloride... [Pg.1727]

Glennon RA et al. (1988) NAN-190 an cU ylpiperazine analog that antagonizes the stimulus effects of the 5-HTlA agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT). Eur J Pharmacol 154(3) 339-341... [Pg.96]

Today, many black developing fluoran compounds having a wide variety of substituents on the amino group at 6 -position are available. These include 2 -anilino-3 -methyl-6 -(Af-methyl-Af- -propylamino)fluoran (53 ... [Pg.177]

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