HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3S,4aS,8aS)-N-(tert-Butyl)decahydroisoquinoline-3-carboxamide → N-tert.butyl-decahydro-2-[2(R)-hydroxy-4-phenyl-3(S)-phthalimidobutyl]-(4aS,8aS)-isoquinoline-3(S)-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3S,4aS,8aS)-N-(tert-Butyl)decahydroisoquinoline-3-carboxamide | HCID 454736 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (2S,3S)-3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-2-hydroxy-4-phenylbutyraldehyde | HCID 86751005 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-tert.butyl-decahydro-2-[2(R)-hydroxy-4-phenyl-3(S)-phthalimidobutyl]-(4aS,8aS)-isoquinoline-3(S)-carboxamide | HCID 9915000 | — |
Reaction Steps
309 mg of (2S,3S)3-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)2-hydroxy-4-phenylbutyraldehyde and 238 mg of N-tert.butyl-decahydro-(4aS,8aS)-isoquinoline-3(S)-carboxamide are dissolved in 5 ml of acetic acid and treated portionwise with 120 mg of sodium cyanoborohydride. After completion of the reaction the mixture is concentrated to dryness, treated with 10 ml of water and extracted with methylene chloride. The extracts are dried and filtered, the filtrate is concentrated and the residue is purified on silica gel with methylene chloride/methanol (95:5). N-tert.Butyl-decahydro-2-[2(R)-hydroxy-4-phenyl-3(S)-phthalimidobutyl]-(4aS,8aS)-isoquinoline-3(S)-carboxamide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05641886 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-274b2ef47e6041999eceee98cbfe21ca |
| Source note | uspto-grants-1997_06 |