HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723249Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 145857714, compound
https://huagongshe.com/reaction/723249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 145857641 | HCID 145857641 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 145857714 | HCID 145857714 | 121.2% |
Reaction Steps
A solution of tetrabutylammonium fluoride (1M in THF, 1 mL, 1 mmol) was added to a solution of {6-amino-3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-2-methyl-biphenyl-4-yl}-carbamic acid 2-trimethylsilanyl-ethyl ester ((Example 294: step f) 86 mg, 0.11 mmol) in THF (1 mL). The solution was heated at 50° C. for 12 h, then the solution was partitioned between EtOAc (50 mL) and water (20 mL). The layers were separated and the organic layer was further extracted with water (5×10 mL) and brine (20 mL). The solution was dried over sodium sulfate and concentrated in vacuo to yield the title compound (71 mg, 84%) which was used without further purification. ESI-MS (m/z): Calcd. for C24H28N4O4S3 (M+H): 533.1; found: 532.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138530B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-7d18eac6239341a483c1a1a9b374e464 |
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| Source note | uspto-grants-2006_11 |
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