HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 23166913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86744241 | HCID 86744241 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23166913 | HCID 23166913 | — |
Reaction Steps
A stirred solution of ethyl (E)-7-{1-(4-fluorophenyl)-3-isopropylpyrrolo[2,1-a]phthalazin-2-yl}-5- hydroxy-3-oxohept-6-enoate (3.98 g) in methanol (120 ml) under an argon atmosphere at 0°-5° C. was treated with sodium borohydride (243 mg). After 3 hours the solution was allowed to warm to room temperature, and was then evaporated to small volume (20 ml). The solution was treated with water (300 ml), and extracted with a mixture of diethyl ether and ethyl acetate (2×250 ml; 1:1 v/v). The combined extracts were dried over magnesium sulphate and evaporated, to give methyl (E)-7-{1-(4-fluorophenyl)-3-isopropylpyrrolo[2,1-a]-phthalazin-2-yl}-3,5-dihydroxyhept-6-enoate, in the form of an orange foam (3.16 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960775 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-57f3267606f5474ca42f7b01c0f8c7cd |
| Source note | uspto-grants-1990_10 |