HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658198Generated: October 30, 2026
Dimethylformamide → HCID 59341359, compound
https://huagongshe.com/reaction/658198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 7-Bromobenzofuran-2-carboxylic acid | HCID 17982651 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59341359 | HCID 59341359 | — |
Reaction Steps
300 mg (1.25 mmol) of 7-bromobenzofuran-2-carboxylic acid, 248 mg (1.25 mmol) of R-3-aminoquinuclidine dihydrochloride, 568 mg (1.494 mmol) of HATU, 579 mg (4.48 mmol) of N,N-diisopropylethylamine and 5 ml of DMF are reacted according to the general procedure (variant B). The product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 30 min. The loaded ion exchanger is washed with DMF, water, methanol, dichloromethane, water, DMF and once again with methanol. The product is eluted with methanol/triethylamine 90:10. The solvent is removed under reduced pressure using a rotary evaporator. The pre-purified product is purified by preparative HPLC. 320 mg (74% of theory) of the title compound are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076355B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-f1467e4795b9450a9a4255b2bfcfedd7 |
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| Source note | uspto-grants-2011_12 |
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