HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228836Generated: October 31, 2026
Ammonium Chloride → 3-(3-Quinolyl)-2-Propyn-1-ol Diisopropyl Carbamate
https://huagongshe.com/reaction/2228836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylcarbamoyl chloride | HCID 87890 | — |
| Reactant | 3-Quinolin-3-ylprop-2-yn-1-ol | HCID 650142 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 3-(3-Quinolyl)-2-Propyn-1-ol Diisopropyl Carbamate | HCID 66669552 | — |
Reaction Steps
To a dry three-necked round-bottom flask equipped with nitrogen inlet and overhead stirrer was charged 3-(3-quinolyl)-2-propyn-1-ol (2 g, 10.8 mmol) (Scheme 1, Compound (3)) in THF (20 ml) and the solution was cooled to 0° C. Potassium t-butoxide (1.34 g, 11.9 mmol) was then added followed by diisopropylcarbamoyl chloride (1.65 g, 11.9 mmol). The mixture was stirred for 2 h at 0° C. and then allowed to warm up to room temperature over a period of 6 hours by which time the reaction was determined to be complete. The reaction mixture was worked up with MTBE (50 ml) and 10% NH4Cl (25 ml) and was concentrated to an orange oil. Yield=3.3 g(100%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417366B2 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-ef471d9aebb84d42aaf00b04f548fd73 |
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| Source note | uspto-grants-2002_07 |
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