Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | Linolenic Acid | HCID 5280934 | — |
| Reactant | N-{5-(3-methoxy-4-beta-methoxyethoxymethoxyphenyl)-2,4-pentadienoyl}-N'-9,12,15-octadecatrieneo yl-1,4-diaminobutane | HCID 53812474 | — |
| Reactant | Water-dioxane--acetic acid | HCID 69202663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54039930 | HCID 54039930 | — |
Reaction Steps
To a solution fo 880 mg (10 mmol) of 1,4-diaminobutane in tetrahydrofuran (20 ml) was added in an argon atmosphere a solutin fo 410 mg (1 mmol) of N-{5-(3-methoxy-4-β-methoxyethoxymethoxyphenyl)-2,4-pentadienoyl}-2-thiothiazolidine in tetrahydrofuran (10 ml) at room temperature over 30 min. The mixture was treated in the same way as in Example 3 to react with 390 mg (1.05 mmol) of α-linolenic acid thiazolidinethionamide. The reaction product was treated in the same way as in Example 3 to hydrolyze N-{5-(3-methoxy-4-β-methoxyethoxymethoxyphenyl)-2,4-pentadienoyl}-N'-9,12,15-octadecatrieneo yl-1,4-diaminobutane with 1,4-dioxane - acetic acid-water (5:4:1). The reaction product was treated in the same way as in Example 3 to give 195 mg (0.35 mmol) of N-{5-(3-methoxy-4-hydroxyphenyl)-2,4-pentadienoyl}-N'- 9,12,15-octadecatrienoyl-1,4-diaminobutane. Spectrophotometric data of the product support the structure shown below. ##STR31##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673684 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-1159ac9b361b47d59daca87cc3e75dbb |
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| Source note | uspto-grants-1987_06 |
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