HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → Methyl 2-(5-iodo-1,2,3,4-tetrahydroisoquinolin-1-yl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoate | HCID 86711344 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 2-(5-iodo-1,2,3,4-tetrahydroisoquinolin-1-yl)propanoate | HCID 86711345 | 101.2% |
Reaction Steps
A mixture of methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoate (1.15 g, 3.35 mmol) in glacial AcOH (12 mL) was treated with NaBH3CN (421 mg, 6.70 mmol) at RTunder N2. The mixture was stirred at RT for 16 h, and then poured onto H2O. The mixture was rendered basic with a 50% aqueous solution of NaOH and extracted with AcOEt. The combined org. phases were then dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (1.17 g) that was used as it is. UPLC-MS: MS 346.1 (M+H+); UPLC rt 0.65 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853203B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-a86b965afe324aba963f5b1888cf739e |
| Source note | uspto-grants-2014_10 |