JPS56122350A - Prostaglandin derivative - Google Patents

Info

Publication number

JPS56122350A

JPS56122350A JP2526480A JP2526480A JPS56122350A JP S56122350 A JPS56122350 A JP S56122350A JP 2526480 A JP2526480 A JP 2526480A JP 2526480 A JP2526480 A JP 2526480A JP S56122350 A JPS56122350 A JP S56122350A

Authority

JP

Japan

Prior art keywords

compound

formula

solution

solvent

dissolving

Prior art date

1980-03-03

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.)

Granted

Links

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• 150000003180 prostaglandins Chemical class 0.000 title 1
• 150000001875 compounds Chemical class 0.000 abstract 6
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
• 239000002904 solvent Substances 0.000 abstract 3
• PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 abstract 2
• 239000003153 chemical reaction reagent Substances 0.000 abstract 2
• 239000000203 mixture Substances 0.000 abstract 2
• YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
• VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 abstract 1
• 239000002253 acid Substances 0.000 abstract 1
• 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
• 229910052805 deuterium Inorganic materials 0.000 abstract 1
• 125000004431 deuterium atom Chemical group 0.000 abstract 1
• 238000003745 diagnosis Methods 0.000 abstract 1
• 238000007865 diluting Methods 0.000 abstract 1
• 239000007789 gas Substances 0.000 abstract 1
• 230000002140 halogenating effect Effects 0.000 abstract 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
• 230000003301 hydrolyzing effect Effects 0.000 abstract 1
• 125000000468 ketone group Chemical group 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 235000006408 oxalic acid Nutrition 0.000 abstract 1
• 238000010979 pH adjustment Methods 0.000 abstract 1
• 239000001632 sodium acetate Substances 0.000 abstract 1
• 235000017281 sodium acetate Nutrition 0.000 abstract 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1