HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553837Generated: October 31, 2026
Propyl mercaptan → HCID 67462595, compound
https://huagongshe.com/reaction/553837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-{(S)-4-tert-butoxycarbonyl-2-[(6-chloro-2-phenyl-pyrimidine-4-carbonyl)-amino]-butyryl}-piperazine-1-carboxylic acid ethyl ester | HCID 86622404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67462595 | HCID 67462595 | — |
Reaction Steps
1-propanethiol (11 μl) was added to a suspension of NaH (4 mg) in anhydrous DMF (0.3 ml) at 0° C. After 1 h stirring at 0° C., 4-{(S)-4-tert-butoxycarbonyl-2-[(6-chloro-2-phenyl-pyrimidine-4-carbonyl)-amino]-butyryl}-piperazine-1-carboxylic acid ethyl ester (50 mg) dissolved in DMF (0.1 ml) was added. The mixture was allowed to warm to RT and was stirred at RT until completion. A NaHCO3 solution was added and the resulting mixture was extracted with DCM. The org. phases were dried (Na2SO4) and evaporated off. The crude was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048881B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-74010be171fb4c4fa3b5a0cbeb2649c3 |
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| Source note | uspto-grants-2011_11 |
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