HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611034Generated: October 31, 2026
1,3-Propanedithiol → HCID 22257960, compound
https://huagongshe.com/reaction/1611034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22257951 | HCID 22257951 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22257960 | HCID 22257960 | 45.1% |
Reaction Steps
5-[(3-Azidopropyl)thio]-3-methyl-1-(2-methylpropyl)-6-(1-naphthalenylmethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (656 mg), 1,3-propanedithiol (100 μl) and triethylamine (400 μl) were dissolved in a mixture of dichloromethane (3 ml) and isopropanol (5 ml). Sodium borohydride (78 mg) was added and the mixture was stirred overnight. The solvents were removed by evaporation then dilute hydrochloric acid was added dropwise until effervescence ceased. The solution was made alkaline with aqueous sodium hydroxide and then extracted with dichloromethane (four times). The extracts were dried, filtered and evaporated. Purification by HPLC (ethanol:dichloromethane 5-40:95-60) followed by trituration with ether-cyclohexane gave the title compound (280 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06984644B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-726fb8803f29479eb5a7ab3a2c3933e2 |
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| Source note | uspto-grants-2006_01 |
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