HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992441Generated: October 30, 2026
tert-Butyl mercaptan → HCID 16753771, compound
https://huagongshe.com/reaction/1992441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 16753769 | HCID 16753769 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 16753771 | HCID 16753771 | — |
Reaction Steps
A bohdan block vessel was charged with 2-methyl-2-propanethiol (20 uL, 0.0002 mol) in DMF (2 mL) and the reaction mixture was degassed 3×. Sodium hydride (0.01 g, 0.0004 mol) was then added and the reaction mixture was stirred at rt for 10 min. 1,3-Dibromo-imidazo[1,5-a]pyrazin-8-ylamine (30 mg, 0.0001 mol) was added to the reaction mixture and the reaction mixture was heated at 70° C. overnight. The reaction mixture turned red in color as the reaction progressed. The reaction mixture was concentrated and purified by prep TLC using a mixture of 7 N5% NH3 in MeOH/DCM to afford the title compound as a white solid. 1H NMR (400 MHz, CD3OD-d4): δ=1.37 (s, 9H), 7.13 (d, J=5.05 Hz, 1H), 7.84 (d, J=5.05 Hz, 1H). MS(ES+): m/z 303.02 (100)[MH+]. HPLC: tR=2.30 min (Open Lynx polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648987B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-c1428dcda5da43c4a5326009fc53d468 |
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| Source note | uspto-grants-2010_01 |
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