HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711343Generated: October 30, 2026
Methyl chloroformate → HCID 118491993, compound
https://huagongshe.com/reaction/711343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 71680612 | HCID 71680612 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118491993 | HCID 118491993 | 45.3% |
Reaction Steps
To a solution of (1S,8aS)-N-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethyl)-N-methyl-6-oxo-1-o-tolylhexahydropyrrolo[1,2-a]pyrazine-2(1H)-carboxamide (300 mg, 0.57 mmol) in anhydrous THF (20 mL) under N2 atmosphere was added LiHMDS (2.3 mL, 1 M in THF, 2.3 mmol) at −60° C. The reaction was stirred for 30 min followed by addition of methyl carbonochloridate (134 mg, 1.43 mmol). After stirring for another 3 h at room temperature. The reaction was quenched with water at 0° C. and then extracted with EA (2×50 mL). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH=20/1 to 10/1) to give the title compound (166 mg, yield: 45.3%); m/z (ES+): 644 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181259B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-656363cfd7624bd099a0c581f59560a3 |
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| Source note | uspto-grants-2015_11 |
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