HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253909Generated: October 31, 2026
1,2-Dichloroethane → HCID 68777526, compound
https://huagongshe.com/reaction/1253909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68777038 | HCID 68777038 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68777526 | HCID 68777526 | 83.7% |
Reaction Steps
To a solution of (R)-5-[3-tert-butoxycarbonylamino-4-(2,4,5-trifluoro-phenyl)-butyryl]-5,6-dihydro-4H-2,5,10b-triaza-benzo[e]azulene-3-carboxylic acid (60 mg, 0.11 mmol) in dry DCM (15 mL), was added HOBT (19 mg, 0.14 mmol), EDC (27 mg, 0.14 mmol) and DIPEA (0.08 mL; 0.46 mmol) and the reaction mixture was stirred for 10 min. Pyrrolidine (0.02 mL, 0.24 mmol) was added and the reaction was stirred at r.t. overnight under nitrogen atmosphere. After the completion of the reaction, as confirmed by TLC, the crude product was extracted with DCM (15 mL) and washed with 10% HCl solution (10 mL) and saturated sodium bicarbonate solution (10 mL). The organic layer was separated washed with water, dried over Na2SO4 and concentrated in vacuo to afford the crude compound, which was purified by column chromatography (silica gel, 3:7 to 9:1 EtOAc:Pet.Ether) to afford (R)-[3-oxo-3-[3-(pyrrolidine-1-carbonyl)-4H,6H-2,5,10b-triaza-benzo[e]azulen-5-yl]-1-(2,4,5-trifluoro-benzyl)-propyl]-carbamic acid tert-butyl ester (55 mg, 83%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455479B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-45a766f0f47c4065bebff363a3316147 |
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| Source note | uspto-grants-2013_06 |
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