HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58840840, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Iodobenzylamine hydrochloride | HCID 2723861 | — |
| Reactant | HCID 87826652 | HCID 87826652 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58840840 | HCID 58840840 | — |
Reaction Steps
65 mg (0.16 mmol) of (3aS,4R,6aR)-4-(2,6-dichloropurin-9-yl)-2,2-dimethyltetrahydrothieno[3,4-d][1,3]dioxole-4-carboxylic acid methyl amide from the aforementioned Experimental Example 10, 55 mg (0.20 mmol) of 3-iodobenzylamine hydrochloride, and 0.065 mL (0.46 mmol) of triethylamine were added to ethanol and stirred at ambient temperature for 3 days. The reaction mixture was distilled under reduced pressure to obtain a concentrate. The concentrate was purified by silica gel column chromatography using the eluant (hexane:ethyl acetate=1:1) to obtain 87 mg (yield: 90%) of (3aS,4R,6aR)-4-[2-chloro-6-(3-iodobenzylamino)purin-9-yl)]-2,2-dimethyltetrahydrothieno[3,4-d][1,3]dioxole-4-carboxylic acid methyl amide as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199127B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-3ad4fbfdca9642ea924e2e23d8ada7d4 |
| Source note | uspto-grants-2007_04 |