Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58748348 | HCID 58748348 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86761677 | HCID 86761677 | — |
Reaction Steps
70.0 mg (0.2 mmol) tert. Butyl (2S,4R)-2-aminomethyl-4-[(5-chloro-thiophene-2-carbonyl)-amino]-pyrrolidine-1-carboxylate are dissolved in 5 ml DCM and combined successively at −10° C. with 15.4 μl (0.2 mmol) acetyl chloride and 67 μl (0.4 mmol) DIPEA. The mixture is stirred for two hours at 0° C. Then it is made weakly acidic by the careful addition of dil. hydrochloric acid and extracted three times with ethyl acetate. The combined organic phases are dried on sodium sulphate, filtered and evaporated down i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309542B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-852156edce2b4988b8a2f78857f1c2fa |
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| Source note | uspto-grants-2012_11 |
|---|