JPS6438050A - Novel production process - Google Patents
Novel production processInfo
- Publication number
- JPS6438050A JPS6438050A JP62194134A JP19413487A JPS6438050A JP S6438050 A JPS6438050 A JP S6438050A JP 62194134 A JP62194134 A JP 62194134A JP 19413487 A JP19413487 A JP 19413487A JP S6438050 A JPS6438050 A JP S6438050A
- Authority
- JP
- Japan
- Prior art keywords
- amino
- peptide
- protecting group
- group
- amino acid
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
Abstract
PURPOSE:To obtain the titled compound useful as a lysine-specific enzyme inhibitor, etc. in high yield and purity at a low cost, by reacting a lysinal derivative with an amino acid or peptide and removing acetal group and amino- protecting group from the resultant acetal compound. CONSTITUTION:The objective lysinal peptide derivative of formula II (A is amino acid residue or peptide residue) can be produced by (1) reacting a compound of formula I (R<1> is amino-protecting group or H; R<2> is amino-protecting group; R<3> and R<4> are 1-4C alkyl or together form a ring) with an amino acid (e.g. valine or leucine) or a peptide to introduce an amino acid or peptide group to the alpha-amino group and (2) removing the amino-protecting group and aldehyde- protecting group with dilute hydrochloric acid or acetic acid, etc., at the same time or by separate means. The side-reaction product can be easily separated by this process.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62194134A JPH0794418B2 (en) | 1987-08-03 | 1987-08-03 | New manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62194134A JPH0794418B2 (en) | 1987-08-03 | 1987-08-03 | New manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6438050A true JPS6438050A (en) | 1989-02-08 |
JPH0794418B2 JPH0794418B2 (en) | 1995-10-11 |
Family
ID=16319473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62194134A Expired - Lifetime JPH0794418B2 (en) | 1987-08-03 | 1987-08-03 | New manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0794418B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992014696A2 (en) * | 1991-02-22 | 1992-09-03 | The Du Pont Merck Pharmaceutical Company | SUBSTITUTED α-AMINOALDEHYDES AND DERIVATIVES |
EP0519748A2 (en) * | 1991-06-21 | 1992-12-23 | Merck & Co. Inc. | Peptidyl derivatives as inhibitors of interleukin-1B converting enzyme |
EP0520336A2 (en) * | 1991-06-19 | 1992-12-30 | FUJIREBIO Inc. | Aldehyde derivatives and their use as calpain inhibitors |
-
1987
- 1987-08-03 JP JP62194134A patent/JPH0794418B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992014696A2 (en) * | 1991-02-22 | 1992-09-03 | The Du Pont Merck Pharmaceutical Company | SUBSTITUTED α-AMINOALDEHYDES AND DERIVATIVES |
EP0520336A2 (en) * | 1991-06-19 | 1992-12-30 | FUJIREBIO Inc. | Aldehyde derivatives and their use as calpain inhibitors |
EP0519748A2 (en) * | 1991-06-21 | 1992-12-23 | Merck & Co. Inc. | Peptidyl derivatives as inhibitors of interleukin-1B converting enzyme |
EP0519748A3 (en) * | 1991-06-21 | 1993-05-05 | Merck & Co. Inc. | Peptidyl derivatives as inhibitors of interleukin-1b converting enzyme |
Also Published As
Publication number | Publication date |
---|---|
JPH0794418B2 (en) | 1995-10-11 |
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