HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474139Generated: October 30, 2026
Sodium Carbonate → HCID 59299295, compound
https://huagongshe.com/reaction/474139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Indolylboronic acid | HCID 2734361 | — |
| Reactant | HCID 66679914 | HCID 66679914 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | HCID 59299295 | HCID 59299295 | 67% |
Reaction Steps
5.19 g (17.4 mmol) of (4S,5R)-4-(5-bromo-pyrimidin-2-yloxy)-1-aza-bicyclo[3.3.1]nonane is dissolved in 200 ml toluene/EtOH 9:1. 5-Indolyl boronic acid (3.47 g, 21.6 mmol), Pd(PPh3)4 (1.04 g, 0.873 mmol) and a soln. of Na2CO3 (7.38 g, 69.6 mmol) in 35 ml H2O is added. The reaction mixture is stirred at 90° C. for 15 h. After cooling to rt the mixture is filtered over hyflo, the filtrate is extracted with water and brine. The aq. layers are reextracted with AcOEt and the combined organic layers are dried over Na2SO4, filtered and the filtrate is evaporated. The resulting crude product is purified by FC (255 g silica gel, eluent AcOEt/MeOH/Et3N 70:27:3) and recrystallization from EtOH to give 3.87 g (67%) (4S,5R)-4-[5-(1H-indol-5-yl)-pyrimidin-2-yloxy]-1-aza-bicyclo[3.3.1]nonane. MS (ES+): m/e=335 (MR+), m.p. 195-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637517B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e5f96f413ea24b4c81a728c70058342e |
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| Source note | uspto-grants-2014_01 |
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