HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804653Generated: October 25, 2026
1,2-Dichloroethane → Tert-butyl (2R,5S)-2-[(R)-hydroxy(phenyl)methyl]-5-(4-{[10-(pyridin-2-ylmethyl)-9,10-diazatricyclo[4.2.1.12,5]dec-9-yl]carbonyl}benzyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1804653
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | (R)-phenyl[(2R,5S)-5-(4-{[4-(1,3-thiazol-4-yl)-piperidin-1-yl]carbonyl}benzyl)pyrrolidine-2-yl]methanol | HCID 50997280 | — |
| Reactant | 4-({(2S,5R)-1-(tert-butoxycarbonyl)-5-[(R)-hydroxy(phenyl)methyl]pyrrolidin-2-yl}methyl)benzoic acid | HCID 67058707 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl (2R,5S)-2-[(R)-hydroxy(phenyl)methyl]-5-(4-{[10-(pyridin-2-ylmethyl)-9,10-diazatricyclo[4.2.1.12,5]dec-9-yl]carbonyl}benzyl)pyrrolidine-1-carboxylate | HCID 67986715 | 42% |
Reaction Steps
To a solution of 4-{((2s,5R)-1-(tert-butoxycarbonyl)-5-[(R)-hydroxy(phenyl)methyl]pyrrolidin-2-yl)methyl}benzoic acid (50 mg, 0.13 mmol) and the title compound from Step B above (37 mg, 0.13 mmol) in 1.5 mL anhydrous DMF was added a 0.5 M solution of HOAt in DMF (0.24 mL, 0.13 mmol) followed by EDC (46 mg, 0.26 mmol) and DIEA (17 μL, 0.13 mmol). The resulting mixture was stirred at RT under nitrogen atmosphere for 16 h. The mixture was washed with water and extracted with dichloromethane (2×5 mL). The organics were combined, dried over sodium sulfate, filtered and concentrated in vacuum. The residue was purified by preparative TLC plate (1000 uM) eluting with 5% MeOH in dichloromethane to afforded the product (32 mg, 42%). ESI-MS calculated for C38H46N4O4: Exact Mass: 622.35. Found 623.38 (MH)+ and 645.33 (MNa)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354403B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-9238bad517944318bc5e049652450a52 |
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| Source note | uspto-grants-2013_01 |
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