Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Reactant | (2S,4S)-4-Aminomethyl-4-fluoro-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester | HCID 68284280 | — |
| Reactant | (2S,4S)-4-Fluoro-4-[(2,2,2-trichloro-ethoxycarbonylamino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester | HCID 71009730 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86673845 | HCID 86673845 | — |
Reaction Steps
To a solution of (2S,4S)-4-aminomethyl-4-fluoro-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester (100 mg, 0.28 mmol) in CH2Cl2 (10 mL) was added Troc-Cl (0.05 mL, 0.34 mmol). The reaction mixture was stirred for 16 h at RT. The reaction mixture was quenched with water, extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, concentrated and purified by flash column chromatography on silica gel (c-hexane/EtOAc 1:1). To a solution of (2S,4S)-4-Fluoro-4-[(2,2,2-trichloro-ethoxycarbonylamino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester (50 mg, 0.09 mmol) and methyl iodide (0.02 mL, 0.28 mmol) in DMF (5 mL) at 0° C. was added sodium hydride (2.50 mg, 0.10 mmol) in portions. The reaction mixture was stirred 90 min at 0° C. and 16 h at RT. The reaction mixture was quenched with water, extracted with EtOAc, washed with brine, dried over Na2SO4, filtered and concentrated. Purification by flash column chromatography on silica gel (c-hexane/EtOAc 1:1). MS (UPLC/MS): 541/543 [M+H]+, 586/587 [M+HCOO]−; tR (HPLC conditions f): 2.66 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085555B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-5a221a7f4ade450eb8d5b4fd14fa6e7d |
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| Source note | uspto-grants-2015_07 |
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