A 5-aminopyrazole of the formula in which R1 represents alkoxycarbonyl, alkenyloxycarbonyl or alkinyloxycarbonyl, and R3, R4, R5, R6, and R7, which are identical or different, represent hydrogen, halogen, cyano, nitro, alkyl, alkoxy, alkylsulphonyl, alkoxycarbonyl or a radical -(X)n-R8 wherein X represents oxygen, sulphur, sulphinyl or sulphyonyl, n represents 0 or 1 and R8 represents halogenoalkyl, with the proviso that at least one of the radicals R3, R4, R5, R6 or R7 represents a radical -(X)n-R8, and R1 does not represent cyano if R1 represents trifluoromethyl, These compounds are intermediates useful in the preparation of herbicidally active substituted 5-acylamino-1-phenylpyrazoles.

Herbicidally active 5-amino-1-phenylpyrazoles of the formula in which R is CN, or an ester or amido group, R1 is an organic radical, R2 is an organic radical, hydrogen or an acyl or thioacyl radical, R3, R4, R5, R6 and R7 can be hydrogen or various organic radicals but at least one is a haloalkyl, haloalkoxy, haloalkylthio, haloalkylsulphinyl or haloalkylsulphonyl radical, but R is not CN at the same time as R5 is CF3. The compounds are intermediates therefor and are also herbicidal.

1. A 2,6-dioxopiperidine selected from the group consisting of n( a ) a compound of the formula: nin which: none of X and Y is C=O and the other of X and Y n( i ) each of R 1 , R 2 , R 3 , and R 4 , independently of yl of 1 to 4 carbon atoms, or alkoxy of 1 to 4 carbon atoms or ( ii ) one of R 1 , R 2 , R 3 , and R 4 is -NHR 5 and the remaining of R 1 , R 2 , R 3 , and R 4 are hydrogen; nR 5 is hydrogen, alkyl of 1 to 8 carbon atoms, or CO-R 7 -CH(R 10 )NR 8 R 9 ; nR 6 is hydrogen, alkyl of 1 to 8 carbon atoms, benzo, chloro, or fluoro; nR 7 is m -phenylene or p -phenylene or -(C n H 2 n )- in which n has a value of 0 to 4; each of R 8 and R 9 taken independently of the other is hydrogen or alkyl of 1 to 8 carbon atoms, or R 8 and R 9 taken together are tetramethylene, pentamethylene, hexamethylene, or -CH 2 CH 2 XCH 2 CH 2 - in which X is -O-, -S- or -NH-; nR 10 is hydrogen, alkyl of 1 to 8 carbon atoms, or phenyl; and n( b ) the acid addition salts of said compounds which contain a nitrogen atom capable of being protonated.

The following are claimed: (A) anthracycline compounds of formula Q-O-R-P (I) Q = a group of formula (i):R = H (sic) or C(O)-(CH2)n-C(O);n = 0-7;R' = NH2; or an aromatic or hydrogenated 5 or 6 membered heterocycle having at least one ring nitrogen, optionally having a butadiene moiety bonded to adjacent carbon atoms to form a bicyclic system;P = H or a peptide; Provided that: (a) where R' is NH2, then R and P are other than H; and (b) where R and P are H, then R' is other than NH2. (B) Conversion of the nitrogen of a primary amino group of an ~a,~b- or ~a,~c-hydroxy primary amine into the nitrogen of a monounsaturated nitrogen-containing heterocyclic compound having 5-6 ring atoms, comprising: (a) treating the hydroxy amine with an excess of a haloaldehyde having an aldehyde carbon, a halo-bearing carbon and having 2 or 3 moieties between the aldehyde carbon and the halo-bearing carbon selected from CH2, CH2CH2 and OCH2; (b) adding an excess (relative to the hydroxyamine) of an organic base; (c) neutralising the base with a weak acid; and (d) treating with a dilute aqueous acid. X' = halo; Y = CH2, OCH2 or CH2-CH2; Z is absent or is CH2.

The invention discloses novel N-(2-nitrophenyl)-2-aminopyrimidine derivatives of the general formula I (I) wherein R1 and R2 are each independently NO2 or CF3, with the proviso that only R1 or R2 can be NO2 R3 is halogen, R4 is hydrogen or the -C(O)R' group, in which R' is C1-C4alkyl which is unsubstituted or substituted by halogen, C1-C3alkoxy or C1-C3alkylthio, R5, R6 and R7 are each independently hydrogen, halogen, nitro, cyano, thiocyano, C1-C12alkyl, C3-C8cycloalkyl, C1-C8alkylthio, C1-C6alkylsulfonyl, C1-C6alkylsulfoxyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6alkenyloxy, C3-C6-haloalkenyloxy, C3-C6alkenylthio, C3-C6alkynyloxy, C3-C6haloalkynyloxy, C1-C8alkyl which is substituted by halogen, cyano and/or C1-C4alkoxy, unsubstituted C1-C8alkoxy or halogen-substituted C1-C8alkoxy, the alkyl moiety of which may be interrupted by one or more single oxygen atoms; or are the Q-(E)n-(X)m-group, in which n is 0 or 1, m is 0 or 1, Q is phenyl which is unsubstituted or substituted by halogen, nitro, C1-C3alkyl, CF3 and/or C1-C3 alkoxy, or is a saturated or unsaturated heterocyclic radical containing one or more hetero atoms, E is a C1-C3alkylene bridge, and X is oxygen or sulfur. Also disclosed are methods of preparing these compounds, and also agrochemical compositions which contain one such compound as active ingredient. The invention further relates to the use of the novel compounds, or, compositions containing them, in agriculture and related fields.

A compound represented by the formula wherein ring A is an optionally substituted 5- to 10-membered aromatic ring; R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; X and Y are the same or different and each is a bound, -O-, -S-, -SO-, -SO?2#191- or -NR3- (R3 is a hydrogen atom or an optionally substituted hydrocarbon group); and L is a divalent hydrocarbon group, or a salt thereof shows a superior peptidase-inhibitory activity and is useful as a prophylactic or therapeutic agent of diabetes and the like.

Chemical patent from PubChem database. Patent Number: AT-E400571-T1. Title: Chemical Synthesis Method. Filing Date: 1992-05-09. Inventors: Yamamoto, Hiroshi, Schmidt, Hans. Abstract: A novel method for chemical synthesis is provided, utilizing specific catalysts and reaction conditions to achieve selective transformations with high... IPC Classifications: C07D, C07F, A61K. This patent covers 45 claims related to 3 chemical compounds. Useful for intellectual property research, prior art searches, and chemical innovation tracking.

1,2,4-Triazol-1-yl-methyl-carbinols of the formula in which Ar is optionally substituted aryl, and Het is optionally substituted heteroaryl with at least 2 different hetero-atoms, or addition products thereof with plant-tolerated acids or metal salts, which possess fungicidal activity.

The invention relates to compounds of formula (I), in which R1, R2, R3, R4, R5 and R6 are defined as cited, in addition to their physiologically compatible salts. The compounds are suitable for use e.g. as hypolipidaemics.