PL55437B1 - - Google Patents
Download PDFInfo
- Publication number
- PL55437B1 PL55437B1 PL111574A PL11157465A PL55437B1 PL 55437 B1 PL55437 B1 PL 55437B1 PL 111574 A PL111574 A PL 111574A PL 11157465 A PL11157465 A PL 11157465A PL 55437 B1 PL55437 B1 PL 55437B1
- Authority
- PL
- Poland
- Prior art keywords
- methyl
- carboalkoxyethyl
- carboalkoxy
- phenyl
- formula
- Prior art date
Links
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 8
- -1 N- (1-methyl-2-carboxyethenyl) - β-phenylalanine ester Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 2
- LDCYZAJDBXYCGN-VIFPVBQESA-N 5-hydroxy-L-tryptophan Chemical compound C1=C(O)C=C2C(C[C@H](N)C(O)=O)=CNC2=C1 LDCYZAJDBXYCGN-VIFPVBQESA-N 0.000 description 1
- LMIQERWZRIFWNZ-UHFFFAOYSA-N 5-hydroxyindole Chemical class OC1=CC=C2NC=CC2=C1 LMIQERWZRIFWNZ-UHFFFAOYSA-N 0.000 description 1
- 229940000681 5-hydroxytryptophan Drugs 0.000 description 1
- CNHHFXMPMWIOOH-LLVKDONJSA-N CC(N[C@H](CC(O)=O)C1=CC=CC=C1)=CC(O)=O Chemical class CC(N[C@H](CC(O)=O)C1=CC=CC=C1)=CC(O)=O CNHHFXMPMWIOOH-LLVKDONJSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000007952 growth promoter Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- LDCYZAJDBXYCGN-UHFFFAOYSA-N oxitriptan Natural products C1=C(O)C=C2C(CC(N)C(O)=O)=CNC2=C1 LDCYZAJDBXYCGN-UHFFFAOYSA-N 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL55437B1 true PL55437B1 (cg-RX-API-DMAC7.html) | 1968-04-25 |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BR112016010788B1 (pt) | Processo para a produção em grande escala de monohidrato de dimesilato de 1-[(2-bromofenil)sulfonil]-5-metoxi-3-[(4-metil-1-piperazinil)metil]-1h- indola | |
| JPH02200674A (ja) | 2―クロロピリジン3―カルボン酸エステルの製法 | |
| JP2021522335A (ja) | トリアゾロピリミジン系化合物の結晶形、塩のタイプおよびその調製方法 | |
| PL55437B1 (cg-RX-API-DMAC7.html) | ||
| SU776559A3 (ru) | Способ получени рацемических или оптически активных производных 1,4бензодиазепин-2-она | |
| US3176017A (en) | Aroylalkyl derivatives of diazabicyclo-nonanes and-decanes | |
| JPH0283371A (ja) | N,n’‐ビス(アルコキシアルキル)‐ピリジン‐2,4‐ジカルボキサミドの製造方法 | |
| Saidov et al. | Development of a new technology for obtaining the Substance of the drug acetamizole | |
| BRPI0612980A2 (pt) | processo para preparaÇço de compostos 3,7-diaza-biciclo[3.3.1] nonano | |
| RU2768824C1 (ru) | 2-(фенил(фенилимино)метил)изоиндолин-1,3-дион и способ его получения | |
| US3705895A (en) | Process for the direct synthesis of styrylpyridinium chlorides | |
| JP3253245B2 (ja) | グアニジン誘導体の製造法、新規中間体およびその製造法 | |
| Wikel et al. | Synthesis of S-Triazole [3, 4-b] benzothiazoles | |
| CN106565657A (zh) | 一种具抗肿瘤活性的橙皮素肉桂酸酯类化合物及其合成方法 | |
| PL55436B1 (cg-RX-API-DMAC7.html) | ||
| CN107619398B (zh) | 2-取代苯并三嗪酮衍生物及其合成方法 | |
| SU1685264A3 (ru) | Способ получени производных пиррола | |
| Ertan et al. | Synthesis of New Annellated Flavonoid Derivatives Possessing Spasmolytic Activity‐VII | |
| US3637737A (en) | 3-aminomethylpyrazolinones | |
| RU2805573C2 (ru) | Способ получения (4s)-4-(4-циано-2-метоксифенил)-5-этокси-2,8-диметил-1,4-дигидро-1,6-нафтиридин-3-карбоксамида посредством разделения рацемата при помощи диастереомерного сложного эфира винной кислоты | |
| RU2084441C1 (ru) | Способ получения кислотно-аддитивных солей труднорастворимых карбоновых кислот и аминов или аминокислот | |
| PL54050B1 (cg-RX-API-DMAC7.html) | ||
| SU202924A1 (cg-RX-API-DMAC7.html) | ||
| SU516688A1 (ru) | Способ получени производных 1,2,4-дитиазепина | |
| PL92578B1 (cg-RX-API-DMAC7.html) |