HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058313Generated: October 30, 2026
1,2-Dichloroethane → HCID 69939642, compound
https://huagongshe.com/reaction/1058313
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- | HCID 85083 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 18672299 | HCID 18672299 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69939642 | HCID 69939642 | 9.4% |
Reaction Steps
EDC (1.51 g, 7.87 mmol) was added to a stirred mixture of 5-chloro-2-[(3-hydroxyazetidin-1-yl)methyl]benzylamine (1.19 g, 5.25 mmol), N-Boc-L-proline (1.13 g, 5.25 mmol) and HOAT (0.36 g, 2.62 mmol) in DMF (9 mL). After 16 h the mixture was concentrated and the residue was partitioned between EtOAc and 10% NaHCO3. The organic layer was washed with water and brine, dried (Na2SO4)and evaporated. The residue was partitioned between EtOAc and 1M citric acid. The aqueous layer was made neutral with NaHCO3 and was extracted into CH2Cl2. The organic layer was evaporated and the residue was purified by chromatography on silica (ammonia saturated CHCl3/MeOH, 95:5) to give N-{5-chloro-2-[(3-hydroxyazetidin-1-yl)methyl]benzyl}-1-(tert-butoxycarbonyl)-L-prolinamide (210 mg) as a glass: MS: 424.5 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515011B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-a6834300403446d6913336c75309e170 |
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| Source note | uspto-grants-2003_02 |
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