GB646048A - Dialkylaminoalkyl ethers of certain polynuclear compounds - Google Patents

Dialkylaminoalkyl ethers of certain polynuclear compounds

Info

Publication number
GB646048A
GB646048A GB32984/47A GB3298447A GB646048A GB 646048 A GB646048 A GB 646048A GB 32984/47 A GB32984/47 A GB 32984/47A GB 3298447 A GB3298447 A GB 3298447A GB 646048 A GB646048 A GB 646048A
Authority
GB
United Kingdom
Prior art keywords
radical
salt
ethers
mentioned
alkylaminoalkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB32984/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GD Searle LLC
Original Assignee
GD Searle LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by GD Searle LLC filed Critical GD Searle LLC
Publication of GB646048A publication Critical patent/GB646048A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/78Ring systems having three or more relevant rings
    • C07D311/80Dibenzopyrans; Hydrogenated dibenzopyrans
    • C07D311/82Xanthenes
    • C07D311/84Xanthenes with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 9
    • C07D311/86Oxygen atoms, e.g. xanthones
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B11/00Diaryl- or thriarylmethane dyes
    • C09B11/28Pyronines ; Xanthon, thioxanthon, selenoxanthan, telluroxanthon dyes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/06Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2603/10Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • C07C2603/12Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
    • C07C2603/18Fluorenes; Hydrogenated fluorenes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Amino - ethers of the general formula A-O-CHn2nNRR1, wherein A represents the benzohydryl or 9-fluoryl radical or the radical <FORM:0646048/IV (b)/1> in which X is a sulphur or oxygen atom or the methylene group, n is 2 or 3, and R and R1 each represent an unsubstituted alkyl group containing not more than 4 carbon atoms, are prepared by heating the corresponding polynuclear alcohol with the appropriate tertiary alkylaminoalkyl halide or a salt thereof, in the presence of caustic alkali, e.g. in the presence of dry, powdered sodium hydroxide. Suitable alkylaminoalkyl halides mentioned are the dimethylamino-, diethylamino-, and dibutylamino-ethyl and propyl chlorides. A number of specific compounds are mentioned. The product may be converted to a salt.
GB32984/47A 1943-10-07 1947-12-15 Dialkylaminoalkyl ethers of certain polynuclear compounds Expired GB646048A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US646048XA 1943-10-07 1943-10-07

Publications (1)

Publication Number Publication Date
GB646048A true GB646048A (en) 1950-11-15

Family

ID=22057072

Family Applications (1)

Application Number Title Priority Date Filing Date
GB32984/47A Expired GB646048A (en) 1943-10-07 1947-12-15 Dialkylaminoalkyl ethers of certain polynuclear compounds

Country Status (2)

Country Link
DE (1) DE857502C (en)
GB (1) GB646048A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3275689A (en) * 1962-08-13 1966-09-27 Merck & Co Inc 3-alkylsulfonyl-5-(tertiaryaminopropylidene)-and 5-hydroxy-5-(tertiaryaminopropyl)-5h-dibenzo[a, d] cycloheptenes
US3622630A (en) * 1968-07-03 1971-11-23 Smith Kline French Lab 10-aminoalkyl-9,10-dihydroanthracenes
US3800044A (en) * 1971-05-10 1974-03-26 Smithkline Corp Pharmaceutical methods using a substituted 10-aminoalkyl-9,10-dihydroanthracene
CN112028780A (en) * 2019-06-03 2020-12-04 北京益民药业有限公司 Purification method of diphenhydramine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3275689A (en) * 1962-08-13 1966-09-27 Merck & Co Inc 3-alkylsulfonyl-5-(tertiaryaminopropylidene)-and 5-hydroxy-5-(tertiaryaminopropyl)-5h-dibenzo[a, d] cycloheptenes
US3622630A (en) * 1968-07-03 1971-11-23 Smith Kline French Lab 10-aminoalkyl-9,10-dihydroanthracenes
US3800044A (en) * 1971-05-10 1974-03-26 Smithkline Corp Pharmaceutical methods using a substituted 10-aminoalkyl-9,10-dihydroanthracene
CN112028780A (en) * 2019-06-03 2020-12-04 北京益民药业有限公司 Purification method of diphenhydramine

Also Published As

Publication number Publication date
DE857502C (en) 1952-12-01

Similar Documents

Publication Publication Date Title
SE7409654L (en)
GB1210230A (en) Bis (acyl-substituted amine-triiodobenzoic acid) compounds for use in x-ray visualization
GB646048A (en) Dialkylaminoalkyl ethers of certain polynuclear compounds
GB647759A (en) Improvements in the manufacture of stilbene derivatives
CA528331A (en) Production of caustic soda
GB1376500A (en) Alkyl-iodo ethers their preparation and pharmaceutical compositions containing them
CA499684A (en) Chemical manufacture of sodium hydrosulfide
GB726786A (en) New salicyclic acid derivatives
CA504544A (en) Conversion of sodium sulphide to sodium sulphite
GB936114A (en) N-(ªá-alkoxy-alkyl)-aniline-disulphonic acid chlorides and their preparation
CA513600A (en) Purification of cellulose with sodium hydroxide
GB578748A (en) Improvements in or relating to phenanthridinium salts
GB1049620A (en) m-bis-(3-methyl-3-butenyl)-benzene and process for its preparation
GB974408A (en) Preparation of allyloxybenzenesulfonates
AU159078B2 (en) Salts of alkyl ethers of 2, 4-diguanidinephenol
GB1359029A (en) Productionof diphenyl ethers
CA524494A (en) Manufacture of dense sodium carbonate
AU158129B2 (en) Improvements relating tothe regeneration of caustic alkali solutions containing mercaptans
GB975812A (en) New sulphonamide derivatives
GB547409A (en) Process for the preparation of 4-acetamido-2-hydroxyphenylarsenoxide
AU210754B2 (en) Use of aromatic ethers as dye assistants
GB741648A (en) Improvements in or relating to coumaran derivatives
ES233667A1 (en) Method of production of a prepared to combat the red spider (Machine-translation by Google Translate, not legally binding)
CA529404A (en) Production of cellulose alkyl ethers
AU130985B2 (en) Magnesium-lithium alloys containing less than 01 % sodium