HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216154Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 145857714, compound
https://huagongshe.com/reaction/2216154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 145857641 | HCID 145857641 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 145857714 | HCID 145857714 | 101.5% |
Reaction Steps
{2-Amino-3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-6-methyl-biphenyl-4-yl}-carbamic acid 2-trimethylsilanyl-ethyl ester (1000 mg, 1.48 mmol, Example 294, step f) was dissolved into THF (25 mL). To this was added TBAF (1M, 1.62 mL, 1.62 mmol) and the reaction was warmed to 40° C. with stirring for 3 hours. Additional TBAF (1.48 mL, 1.48 mmol) was added and the reaction was stirred at rt overnight. The solvents were removed in vacuo, the residue was dissolved into EtOAc and washed with water several times (5 washes). The combined organic layers were dried (MgSO4) and the solvents were removed in vacuo resulting in the title compound as a yellow solid (800 mg, 100%). 1H-NMR (CDCl3): δ: 8.03 (s, 1H), 7.95–7.93 (m, 1H), 7.89–7.88 (m, 1H), 7.59–7.53 (m, 2H), 6.08 (m, 1H), 5.99 (m, 1H), 2.55 (s, 3H), 1.85 (s, 3H), 1.52 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07109354B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-6343862bdcdf4c8eb9300f5da1c16ce7 |
|---|
| Source note | uspto-grants-2006_09 |
|---|