BE487293A - - Google Patents
Info
- Publication number
- BE487293A BE487293A BE487293DA BE487293A BE 487293 A BE487293 A BE 487293A BE 487293D A BE487293D A BE 487293DA BE 487293 A BE487293 A BE 487293A
- Authority
- BE
- Belgium
- Prior art keywords
- salt
- cyanamide
- guanidine
- isopropylguanidine
- salts
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 claims description 30
- 239000011780 sodium chloride Substances 0.000 claims description 30
- UZEKTDVGUQCDBI-UHFFFAOYSA-N 2-propan-2-ylguanidine Chemical compound CC(C)NC(N)=N UZEKTDVGUQCDBI-UHFFFAOYSA-N 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 7
- 150000001447 alkali salts Chemical class 0.000 claims description 6
- 239000012047 saturated solution Substances 0.000 claims description 6
- 150000001912 cyanamides Chemical class 0.000 claims description 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 4
- XZMCDFZZKTWFGF-UHFFFAOYSA-N carbodiimide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- RDOXTESZEPMUJZ-UHFFFAOYSA-N Anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 239000003518 caustics Substances 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 150000002357 guanidines Chemical class 0.000 claims 3
- 238000010908 decantation Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000000047 product Substances 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- XMIWFFMIJCOJLR-UHFFFAOYSA-N 2-propan-2-ylguanidine;sulfuric acid Chemical compound OS(O)(=O)=O.CC(C)N=C(N)N XMIWFFMIJCOJLR-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- LDKDGDIWEUUXSH-UHFFFAOYSA-N Thymolphthalein Chemical compound C1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3C(=O)O2)C=2C(=CC(O)=C(C(C)C)C=2)C)=C1C LDKDGDIWEUUXSH-UHFFFAOYSA-N 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- GGIDNUBNZYGILQ-UHFFFAOYSA-N chloro(phenyl)cyanamide Chemical compound N#CN(Cl)C1=CC=CC=C1 GGIDNUBNZYGILQ-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000005712 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- JLXXLCJERIYMQG-UHFFFAOYSA-N phenylcyanamide Chemical compound N#CNC1=CC=CC=C1 JLXXLCJERIYMQG-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE487293A true BE487293A (ja) |
Family
ID=132768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE487293D BE487293A (ja) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE487293A (ja) |
-
0
- BE BE487293D patent/BE487293A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BE1008403A4 (fr) | Procede de cristallisation d'iopamidol. | |
EP0377381A1 (fr) | Procédé de préparation du phényl-1 diéthylaminocarbonyl-1 phtalimidométhyl-2 cyclopropane Z | |
BE487293A (ja) | ||
EP0071500B1 (fr) | Procédé de préparation d'amino-4 butyramide | |
CH277982A (fr) | Procédé de préparation du sel de la p-chlorophényl-cyanamide et de l'isopropylguanidine. | |
CH594650A5 (en) | Antiinflammatory (1,2)-benzothiazine derivs. prepn. | |
CA2082286C (fr) | Nouveau procede de preparation de la lactone de l'acide 1r,cis 2,2-dimethyl 3-formyl cyclopropane-1-carboxylique et intermediaires | |
EP0124407B1 (fr) | Procédé de préparation d'acides alkanoiques | |
EP0132201A2 (fr) | Procédé de préparation du phénylpyruvate de sodium monohydraté cristallisé | |
CH476658A (fr) | Procédé pour la préparation d'une dihydroxy-dicétone | |
BE897708A (fr) | Procede de preparation de 2-benzothiazole-sulfenamides a empechement sterique | |
BE504827A (ja) | ||
CH330478A (fr) | Procédé de préparation de nouveaux thiodérivés de colchicéines | |
CH257402A (fr) | Procédé pour la préparation de 5-nitro-anilines présentant en position 2 un reste-OR. | |
BE837031A (fr) | Procede de preparation d'acide 3,6- dichloropicolinique | |
CH406190A (fr) | Procédé de préparation de l'acide hydroxy-10 décène-2 oïque trans | |
CH378903A (fr) | Procédé de préparation d'un dérivé de la dichloracétanilide | |
BE549645A (ja) | ||
BE430451A (ja) | ||
BE452466A (ja) | ||
BE671514A (ja) | ||
CH432512A (fr) | Procédé de préparation de stéroïdes 21-bromés | |
BE517207A (ja) | ||
CH309458A (fr) | Procédé de préparation du bromhydrate de chlortétracycline. | |
BE540075A (ja) |