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    • 3. 发明专利
    • PROCESS FOR PRODUCING POLYALKYL-1-OXA-DIAZA-SPIRODECANE DERIVATIVES
    • HUT71255A
    • 1995-11-28
    • HU9500472
    • 1995-02-17
    • HOECHST AG
    • GAA KARLNOWY GUENTERSCHMAILZL GEORG
    • C07D498/10C07D519/00C08G73/06
    • The prodn. of polyalkyl-1-oxa-diazaspirodecane cpds. of formula (I) comprises reacting a cpd. of formula (VI) with an epihalohydrin of formula (V) in the mole ratio of (1:1)-(1:10), in organic solvent and in the presence of alkali hydroxide (AOH) as the soln. catalyst and then (for n > 1) heating the resulting epoxide (VI) at 100-240 degrees C. The AOH consists of 1-20 moles solid alkali metal hydroxide or a mixt. thereof with water in the wt. ratio of (1:9)-(9:1) and the solvent comprises alcohol(s) and opt. an inert organic solvent. n = 1-50; Y = a gp. of formula (II) or (III) (indices 3 and 4 indicate ring positions in I, with the N atom attached to a CH2 gp. in the propylene-2-oxy gp.); R = H, O, NO gp., 1-12 C alkyl or alkoxy, allyl, 1-22 C acyl, benzyl or 3-12 C cycloalkoxy; R = R = H or 1-5 C alkyl and R = Me; or R = H or 1-5 C alkyl and R + R + attached C atoms = 5-6 C cycloalkyl gp. or a gp. of formula; R , R = H, 1-30 C alkyl or 7-12 C phenylalkyl (opt. substd. with Cl or 1-4 C alkyl); or R + R + attached C atom = 5-18 C cycloalkyl (opt. substd. with up to four 1-4 C alkyl gps.) or a gp. of formula; if n = 1, R is absent, i.e. the O and the terminal CH2 gp. form an oxirane ring; if n > 1, R = H or 1-22 C acyl; or R may be absent in the terminal monomer unit with an oxirane ring present as above; HX = acid residue or a salt thereof with a protic acid; Hal = Cl, Br or I.
    • 7. 发明专利
    • PROCESS FOR PRODUCING POLYALKYL-1-OXA-DIAZA-SPIRODECANE DERIVATIVES
    • HU214962B
    • 1998-08-28
    • HU9500472
    • 1995-02-17
    • HOECHST AG
    • GAA KARLNOWY GUENTERSCHMAILZL GEORG
    • C07D498/10C07D519/00C08G73/06
    • The prodn. of polyalkyl-1-oxa-diazaspirodecane cpds. of formula (I) comprises reacting a cpd. of formula (VI) with an epihalohydrin of formula (V) in the mole ratio of (1:1)-(1:10), in organic solvent and in the presence of alkali hydroxide (AOH) as the soln. catalyst and then (for n > 1) heating the resulting epoxide (VI) at 100-240 degrees C. The AOH consists of 1-20 moles solid alkali metal hydroxide or a mixt. thereof with water in the wt. ratio of (1:9)-(9:1) and the solvent comprises alcohol(s) and opt. an inert organic solvent. n = 1-50; Y = a gp. of formula (II) or (III) (indices 3 and 4 indicate ring positions in I, with the N atom attached to a CH2 gp. in the propylene-2-oxy gp.); R = H, O, NO gp., 1-12 C alkyl or alkoxy, allyl, 1-22 C acyl, benzyl or 3-12 C cycloalkoxy; R = R = H or 1-5 C alkyl and R = Me; or R = H or 1-5 C alkyl and R + R + attached C atoms = 5-6 C cycloalkyl gp. or a gp. of formula; R , R = H, 1-30 C alkyl or 7-12 C phenylalkyl (opt. substd. with Cl or 1-4 C alkyl); or R + R + attached C atom = 5-18 C cycloalkyl (opt. substd. with up to four 1-4 C alkyl gps.) or a gp. of formula; if n = 1, R is absent, i.e. the O and the terminal CH2 gp. form an oxirane ring; if n > 1, R = H or 1-22 C acyl; or R may be absent in the terminal monomer unit with an oxirane ring present as above; HX = acid residue or a salt thereof with a protic acid; Hal = Cl, Br or I.
    • 9. 发明专利
    • METHOD OF OBTAINING POLYALKYL-1-OXA-DIAZASPIRODECANE COMPOUNDS
    • PL307323A1
    • 1995-08-21
    • PL30732395
    • 1995-02-17
    • HOECHST AG
    • GAA KARLNOWY GUENTERSCHMAILZL GEORG
    • C07D498/10C07D519/00C08G73/06C07D491/12
    • The prodn. of polyalkyl-1-oxa-diazaspirodecane cpds. of formula (I) comprises reacting a cpd. of formula (VI) with an epihalohydrin of formula (V) in the mole ratio of (1:1)-(1:10), in organic solvent and in the presence of alkali hydroxide (AOH) as the soln. catalyst and then (for n > 1) heating the resulting epoxide (VI) at 100-240 degrees C. The AOH consists of 1-20 moles solid alkali metal hydroxide or a mixt. thereof with water in the wt. ratio of (1:9)-(9:1) and the solvent comprises alcohol(s) and opt. an inert organic solvent. n = 1-50; Y = a gp. of formula (II) or (III) (indices 3 and 4 indicate ring positions in I, with the N atom attached to a CH2 gp. in the propylene-2-oxy gp.); R = H, O, NO gp., 1-12 C alkyl or alkoxy, allyl, 1-22 C acyl, benzyl or 3-12 C cycloalkoxy; R = R = H or 1-5 C alkyl and R = Me; or R = H or 1-5 C alkyl and R + R + attached C atoms = 5-6 C cycloalkyl gp. or a gp. of formula; R , R = H, 1-30 C alkyl or 7-12 C phenylalkyl (opt. substd. with Cl or 1-4 C alkyl); or R + R + attached C atom = 5-18 C cycloalkyl (opt. substd. with up to four 1-4 C alkyl gps.) or a gp. of formula; if n = 1, R is absent, i.e. the O and the terminal CH2 gp. form an oxirane ring; if n > 1, R = H or 1-22 C acyl; or R may be absent in the terminal monomer unit with an oxirane ring present as above; HX = acid residue or a salt thereof with a protic acid; Hal = Cl, Br or I.