HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338116Generated: October 30, 2026
1-Chloro-N,N-2-trimethylpropenylamine → HCID 89832293, compound
https://huagongshe.com/reaction/338116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | HCID 89823284 | HCID 89823284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89832293 | HCID 89832293 | 198.7% |
Reaction Steps
Racemic tert-butyl 3-(benzoylcarbamothioylamino)-3-(2-fluorophenyl)-4-(hydroxymethyl)pyrrolidine-1-carboxylate (2.1 g, 4.39 mmol) is dissolved in dichloromethane (75 mL) and partitioned in equal portions between three reaction vessels. The reaction vessels are cooled to 0° C., and to each vessel is added drop wise 1-chloro-N,N,2-trimethylpropenylamine (2.0 mL, 15 mmol). The reactions are warmed to 22° C., and stirred for 4 hours. The contents of each vessel are passed through a 10 g silica gel plug, washed with methanol (30 ml), and the solvent removed under reduced pressure. The residues are purified by reverse phase HPLC eluting with a gradient of 5 to 100% acetonitrile in 10 mM ammonium bicarbonate solution w/5% methanol (pH 10.0) to give the title compound (3.1 g). ES/MS (m/e): 356 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889856B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-c54b29483b3c4296957d57ca59ee85e6 |
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| Source note | uspto-grants-2014_11 |
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