HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046147Generated: October 30, 2026
Methyl chloroformate → HCID 67992236, compound
https://huagongshe.com/reaction/2046147
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Aripiprazole | HCID 60795 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | HCID 67992236 | HCID 67992236 | — |
Reaction Steps
To a solution of diisopropylamine (0.99 mL, 7.02 mmol) in 2-methyltetrahydrofuran (33 mL) at −5° C. was added n-BuLi (2.67 mL, 2.5 M in hexanes, 6.69 mmol) slowly. After 20 minutes, the reaction was cooled to −78° C. and aripiprazole (1.50 g, 3.34 mmol) was added. After a further 10 minutes, methylchloroformate (0.65 mL, 8.36 mmol) was added. The reaction was held at −78° C. for 2 hours before allowing to warm to room temperature. After 2 hours the reaction was quenched with saturated aqueous ammonium chloride solution (30 mL) and extracted with ethyl acetate (2×30 mL). The organics were combined, washed with saturated aqueous sodium hydrogen carbonate solution (30 mL), brine (30 mL), dried over MgSO4 and concentrated. The crude product was purified by column chromatography on silica eluting with 1:1 ethyl acetate to dichloromethane to 10% methanol in 1:1 ethyl acetate to dichloromethane to give the product. The product was triturated in heptane to remove aliphatic impurities and then filtered to afford Compound-74 (0.824 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592427B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-88147804eb8e41508909dcd05edb3d84 |
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| Source note | uspto-grants-2013_11 |
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