HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504332Generated: October 29, 2026
Dimethylformamide → HCID 66662432, compound
https://huagongshe.com/reaction/504332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 66662046 | HCID 66662046 | — |
| Reactant | HCID 66662416 | HCID 66662416 | — |
| Product | HCID 66662432 | HCID 66662432 | — |
Reaction Steps
HCl in dioxane (4.0 M, 1 mL) was added to tert-butyl 4-fluoro-3-oxo-1′H,3H-spiro[furo[3,4-c]pyridine-1,3′-pyrrolidine]-1′-carboxylate (25.8 mg, 0.0000837 mol). The reaction mixture was stirred at room temperature for 30 minutes before the volatiles was removed to afford the free amine (hydrochloric acid salt), which was subsequently used in the coupling reaction. 4-Methylmorpholine (50 μL, 0.0004 mol) was added to a mixture of 1-quinolin-4-ylcyclopropanecarboxylic acid (17.8 mg, 0.0000837 mol), 4-fluoro-3H-spiro[furo[3,4-c]pyridine-1,3′-pyrrolidin]-3-one dihydrochloride (23.5 mg, 0.0000837 mol), and (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (45.7 mg, 0.0000879 mol) in N,N-dimethylformamide (0.5 mL, 0.006 mol). The reaction mixture was stirred at room temperature for 2 hours. The crude product was purified by prep-LCMS. LC/MS: 402.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776874B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-6cbf5f6b607b46b795a92e56ade659c7 |
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| Source note | uspto-grants-2010_08 |
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