GB951940A - A process for producing aromatic ª-acylaminoalkyl and aminoalkyl compounds - Google Patents
A process for producing aromatic ª-acylaminoalkyl and aminoalkyl compoundsInfo
- Publication number
- GB951940A GB951940A GB16753/60A GB1675360A GB951940A GB 951940 A GB951940 A GB 951940A GB 16753/60 A GB16753/60 A GB 16753/60A GB 1675360 A GB1675360 A GB 1675360A GB 951940 A GB951940 A GB 951940A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- acetamide
- preparation
- describes
- compounds
- 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
Links
- 125000003118 aryl group Chemical group 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 125000004103 aminoalkyl group Chemical group 0.000 title 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 230000007062 hydrolysis Effects 0.000 abstract 3
- 238000006460 hydrolysis reaction Methods 0.000 abstract 3
- KUFFULVDNCHOFZ-UHFFFAOYSA-N 2,4-xylenol Chemical compound CC1=CC=C(O)C(C)=C1 KUFFULVDNCHOFZ-UHFFFAOYSA-N 0.000 abstract 2
- KPRZOPQOBJRYSW-UHFFFAOYSA-N 2-(aminomethyl)phenol Chemical compound NCC1=CC=CC=C1O KPRZOPQOBJRYSW-UHFFFAOYSA-N 0.000 abstract 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 2
- 125000004442 acylamino group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- -1 alkylidene bisamide Chemical compound 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000001923 cyclic compounds Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- RRSCVDMNAXVDSV-UHFFFAOYSA-N n-(acetamidomethyl)acetamide Chemical compound CC(=O)NCNC(C)=O RRSCVDMNAXVDSV-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- XDYNOBXKXBQMTO-UHFFFAOYSA-N 1-(5-amino-8-hydroxy-2-methyl-2H-quinolin-1-yl)ethanone Chemical compound C(C)(=O)N1C(C=CC2=C(C=CC(=C12)O)N)C XDYNOBXKXBQMTO-UHFFFAOYSA-N 0.000 abstract 1
- DAJRJDKWBYJJTB-UHFFFAOYSA-N 2-(azaniumylmethyl)-4-nitrophenolate Chemical compound NCC1=CC([N+]([O-])=O)=CC=C1O DAJRJDKWBYJJTB-UHFFFAOYSA-N 0.000 abstract 1
- BPEXTIMJLDWDTL-UHFFFAOYSA-N 2`-Methylacetanilide Chemical compound CC(=O)NC1=CC=CC=C1C BPEXTIMJLDWDTL-UHFFFAOYSA-N 0.000 abstract 1
- INNIENBZXVVRGC-UHFFFAOYSA-N 3-phenylpentanediamide Chemical compound NC(=O)CC(CC(N)=O)C1=CC=CC=C1 INNIENBZXVVRGC-UHFFFAOYSA-N 0.000 abstract 1
- IDKMYDUUWYPLCR-UHFFFAOYSA-N 4-(azaniumylmethyl)-2-carboxyphenolate Chemical compound NCC1=CC=C(O)C(C(O)=O)=C1 IDKMYDUUWYPLCR-UHFFFAOYSA-N 0.000 abstract 1
- QHLHGNNEBLNVKT-UHFFFAOYSA-N 5-[acetyl(methyl)amino]-2-hydroxybenzoic acid Chemical compound C(C)(=O)N(C=1C=CC(=C(C(=O)O)C=1)O)C QHLHGNNEBLNVKT-UHFFFAOYSA-N 0.000 abstract 1
- YTEAFURBNAEAQX-UHFFFAOYSA-N N-[(2-hydroxy-3,5-dimethylphenyl)methyl]formamide Chemical compound OC1=C(CNC=O)C=C(C=C1C)C YTEAFURBNAEAQX-UHFFFAOYSA-N 0.000 abstract 1
- GKIAWHBTRJNALN-UHFFFAOYSA-N N-[(2-hydroxy-3,5-dimethylphenyl)methyl]propanamide Chemical compound OC1=C(CNC(CC)=O)C=C(C=C1C)C GKIAWHBTRJNALN-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- KVIZYCBDCWXNOQ-UHFFFAOYSA-N bmy-40660 Chemical compound CC(=O)NCC1=CC=C(O)C=C1 KVIZYCBDCWXNOQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 150000003956 methylamines Chemical group 0.000 abstract 1
- QPJQPYQZFKFTHG-UHFFFAOYSA-N n-(formamidomethyl)formamide Chemical compound O=CNCNC=O QPJQPYQZFKFTHG-UHFFFAOYSA-N 0.000 abstract 1
- SKIMPHYSGGMGFO-UHFFFAOYSA-N n-[(2-hydroxy-5-nitrophenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC([N+]([O-])=O)=CC=C1O SKIMPHYSGGMGFO-UHFFFAOYSA-N 0.000 abstract 1
- CLTHXCBZMXABDP-UHFFFAOYSA-N n-[(2-hydroxyphenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC=CC=C1O CLTHXCBZMXABDP-UHFFFAOYSA-N 0.000 abstract 1
- NGXAWGOVQDFBPW-UHFFFAOYSA-N n-[(propanoylamino)methyl]propanamide Chemical compound CCC(=O)NCNC(=O)CC NGXAWGOVQDFBPW-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000012044 organic layer Substances 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract 1
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/38—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to acyclic carbon atoms and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1549859 | 1959-05-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB951940A true GB951940A (en) | 1964-03-11 |
Family
ID=11890456
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB16753/60A Expired GB951940A (en) | 1959-05-13 | 1960-05-12 | A process for producing aromatic ª-acylaminoalkyl and aminoalkyl compounds |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH394230A (enrdf_load_stackoverflow) |
| FR (1) | FR449M (enrdf_load_stackoverflow) |
| GB (1) | GB951940A (enrdf_load_stackoverflow) |
-
1960
- 1960-05-12 CH CH544860A patent/CH394230A/de unknown
- 1960-05-12 GB GB16753/60A patent/GB951940A/en not_active Expired
- 1960-08-30 FR FR837142A patent/FR449M/fr active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CH394230A (de) | 1965-06-30 |
| FR449M (enrdf_load_stackoverflow) | 1961-04-24 |
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