HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729090Generated: November 1, 2026
Diisopropylethylamine → HCID 54338434, compound
https://huagongshe.com/reaction/1729090
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-adamantyl Chloroformate | HCID 10878537 | — |
| Reactant | HCID 54211748 | HCID 54211748 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54338434 | HCID 54338434 | — |
Reaction Steps
To a stirred solution of 2-[9-(methylsulfonyl)-β-carbolin-3-yl]-alanine methylester (0.5 g, 1.4 mmol) in THF (10 mL) was added 2-adamantyloxycarbonyl chloride (345 rag, 1.7 mmol) and the solution was treated with diisopropyl ethylamine (219 mg, 1.7 mmol) in THF (5 mL). The reaction mixture was stirred for 4 hours at room temperature, evaporated in vacuum and partitioned between ethyl acetate (100 mL) and water (50 mL). The organic layer was separated,washed successively with 7.5% citric acid solution (50 mL), 8% NaHCO3 solution (50 mL) and then dried over Na2SO4. The solvent was evaporated in vacuum and N-(2-adamantyloxy-carbonyl)-2-[9-(methylsulfonyl)-β-carbolin-3-yl]-alanine methylester was isolated as a yellow oil which solidified upon drying(0.73 g, 97.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05331006 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-d258563f8b1848adb21822d41bdb624d |
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| Source note | uspto-grants-1994_07 |
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