HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785049Generated: October 28, 2026
Trifluoroacetic acid → HCID 67278023, compound
https://huagongshe.com/reaction/1785049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 57594128 | HCID 57594128 | — |
| Reactant | 1,1-dimethylethyl (4R)-4-(([(1,1-dimethylethyl)oxy]carbonyl}amino)-5-[4-(8-methylimidazo[1,2-a]pyridin-2-yl)phenyl]pentanoate | HCID 67278371 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67278023 | HCID 67278023 | 61% |
Reaction Steps
To a solution of 1,1-dimethylethyl (4R)-4-(([(1,1-dimethylethyl)oxy]carbonyl}amino)-5-[4-(8-methylimidazo[1,2-a]pyridin-2-yl)phenyl]pentanoate (1.35 g, 2.82 mmol) in CH2Cl2 (14 mL) was added trifluoroacetic acid (10 mL) followed by triethylsilane (2.5 equiv, 7.04 mmol). The reaction was stirred for 45 minutes at room temperature and then concentrated in vacuo. DMF (35 mL) was added to the residue followed by diisopropylamine (14.7 mL, 84.51 mmol) under nitrogen. The reaction was stirred for 5 minutes and pentafluorophenyl 3-chloro-4-[(1-methylethyl)oxy]benzoate (1.1 equiv, 3.10 mmol) was added. The reaction was stirred for 45 minutes and then concentrated in vacuo. Ethyl acetate (50 mL) was added to the residue and it was washed with H2O (30 mL). The aqueous layer was extracted with EtOAc (20 mL) and the combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification by silica gel chromatography (Analogix IF280, 25-100% EtOAc/hexanes) provided the title compound as a white foamy solid (61%). ESMS [M+H]+=520.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504413B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-d72ee98388eb46d4be26dc716f355c6d |
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| Source note | uspto-grants-2009_03 |
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