HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46197Generated: October 29, 2026
Sodium methanethiolate → HCID 67287391, compound
https://huagongshe.com/reaction/46197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 2-Chloro-5-(2-chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-1,3,4-thiadiazole | HCID 67286955 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67287391 | HCID 67287391 | 77% |
Reaction Steps
To a solution of 2-chloro-5-(2-chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)-1,3,4-thiadiazole (419 mg, 0.55 mmol) from Step 2 in tetrahydrofuran (10 mL) was added sodium methanethiolate (77 mg, 1.1 mmol). The resulting mixture was stirred at ambient temperature overnight. After cooling to 0° C., the reaction was quenched with hydrochloric acid (1.0 M) and diluted with ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on Biotage® purification apparatus (silica gel, 10 to 60% ethyl acetate in hexanes) to yield the title compound (331 mg, 0.42 mmol, 77%) as a yellow oil. MH+ 779.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541380B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-1b8032a7eb284b2a98884ad809915433 |
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| Source note | uspto-grants-2013_09 |
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