HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175136Generated: October 29, 2026
1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → Carbamic acid, N-[1-(6-hydroxy-3-quinolinyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/2175136
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | tert-butyl N-(pyrrolidin-3-yl)carbamate | HCID 2757234 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 3-Bromoquinolin-6-yl acetate | HCID 68530047 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Carbamic acid, N-[1-(6-hydroxy-3-quinolinyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl ester | HCID 86696256 | 12% |
Reaction Steps
A mixture of Intermediate A (1.50 g, 5.07 mmol), tert-butyl pyrrolidin-3-ylcarbamate (1.13 g, 6.09 mmol), Pd2(dba)3 (0.232 g, 0.254 mmol), Xantphos (0.294 g, 0.507 mmol) and KOtBu (1.14 g, 10.2 mmol) in DMF (15 mL) was bubbled with argon for 20 min. The result mixture was heated at 110° C. overnight. The solution was cooled to rt and the solvent was removed under reduced pressure. The residue was diluted with water, extracted with DCM three times. The combined organic phase was dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography (eluting with 5% MeOH in DCM) to give the title compound as yellow solid (0.2 g, yield 11%). LCMS (method N): [M+H]+=330, tR=1.93 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062045B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-dc9dd3fcf64d4589bb1e0468547c6b64 |
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| Source note | uspto-grants-2015_06 |
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