HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899146Generated: October 29, 2026
Dichloromethane → HCID 11503305, compound
https://huagongshe.com/reaction/899146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane | HCID 16036407 | — |
| Reactant | HCID 86616242 | HCID 86616242 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11503305 | HCID 11503305 | 52.4% |
Reaction Steps
3-Benzyl-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane (0.18 g, 0.82 mmol; see WO 01/28992) and toluene-4-sulfonic acid 2-{1-[2-(4-cyanophenoxy)ethyl]-ureido}ethyl ester (0.50 g, 1.24 mmol; see Preparation D above) were mixed in dry acetonitrile (15 mL) and stirred at 60° C. overnight. DCM (10 mL) was added, together with 0.5 g of PS—NCO (polymer-supported isocyanate). The mixture was stirred for 2 h, then filtered and evaporated. The crude product was put on a SCX-II (cation exchanger)-plug, which plug was then eluted with DCM:MeOH (NH3-saturated), 80:20. The product was further purified on a Horizon prep. column (40 g, A: DCM(1% MeOH), B: DCM/MeOH(NH3-sat.), 80:20. Gradient 0-30% B over 1080 mL). The product was then further purified by prep. HPLC and finally extracted with DCM/Na2CO3 (aq.) to give 193 mg (51.9%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354917B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-b2feadb2ce3f4958ad063397c84e585b |
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| Source note | uspto-grants-2008_04 |
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