HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969711Generated: November 1, 2026
Dichlorodimethylsilane → 2,6-Dichloropurine
https://huagongshe.com/reaction/969711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichlorodimethylsilane | HCID 6398 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | HCID 10149094 | HCID 10149094 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 2,6-Dichloropurine | HCID 5324412 | 72.6% |
Reaction Steps
9-Acetyl-2-amino-6-chloropurine (2.50 g, 11.8 mmol), dichlorodimethylsilane (4.57 g, 35.4 mmol), benzyltriethylammonium chloride (0.16 g, 0.70 mmol) and isoamyl nitrite (2.07 g, 17.7 mmol) were added to o-dichlorobenzene (10 ml), and the mixture was heated to 25-30° C. and stirred for 8 hr. After the completion of the reaction, the mixture was filtrated. The obtained crystals were diluted with water (4.0 ml), and the reaction mixture was added dropwise to 2M aqueous sodium hydroxide solution (20 ml) and partitioned. The aqueous layer was adjusted to pH 4-5 with 35% hydrochloric acid. After aging under ice-cooling for 1 hr, the mixture was filtrated, and the obtained crystals were dried under reduced pressure at 80° C. to give 2,6-dichloropurine as a white powder (1.62 g, yield 72.6%). The properties of the obtained compound were the same as in Example 1(2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07307167B2 |
|---|
| Source dataset | uspto-grants-2007_12 |
|---|
| ORD ID | ord-575825576c19492d8de4acc092c51aeb |
|---|
| Source note | uspto-grants-2007_12 |
|---|