HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184365Generated: November 1, 2026
TBAF tetrahydrofuran → HCID 68106416, compound
https://huagongshe.com/reaction/1184365
Participants
| Role | Name | HCID | Charge |
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| Reactant | TBAF tetrahydrofuran | HCID 11078149 | — |
| Reactant | HCID 68106574 | HCID 68106574 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68106416 | HCID 68106416 | 78.6% |
Reaction Steps
N-[(3-{[tert-Butyl (dimethyl)silyl]oxy}pyrrolidin-1-yl)sulfonyl]-2-{[(3,5-dimethoxy-4-methylbenzoyl)(3-phenylpropyl)amino]methyl}-1,3-thiazole-4-carboxamide (580 mg) was added to THF (10 mL), and subsequently, a 1 M TBAF/THF solution (2.02 mL) was added dropwise thereto, followed by stirring at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the obtained residue was neutralized by the addition of an appropriate amount of 1 M hydrochloric acid, and then extracted with CHCl3 several times. The organic layer was washed with brine and dried over MgSO4, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (CHCl3:MeOH=20:1) to obtain 2-{[(3,5-dimethoxy-4-methylbenzoyl)(3-phenylpropyl)amino]methyl}-N-[(3-hydroxypyrrolidin-1-yl)sulfonyl]-1,3-thiazole-4-carboxamide (383 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669246B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-841a1ce6900849f084c246a723050290 |
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| Source note | uspto-grants-2014_03 |
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