Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Reactant | HCID 11292979 | HCID 11292979 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11202178 | HCID 11202178 | 43% |
Reaction Steps
To a stirred solution of benzo[1,2,5]thiadiazole-4-sulfonic acid [5-amino-2-(piperidine-1-carbonyl)-phenyl]-amide (EXAMPLE 24; 25 mg, 0.06 mmol) in glacial acetic acid (3 mL) was added 2,5-dimethoxytetrahydrofuran (8 μL, 0.06 mmol). The reaction mixture was heated to 120° C. for 45 min after which it was cooled to room temperature. The mixture was taken up to 4 mL of DCM and washed with water. The organic layer was removed, dried and purified by preparative reversed-phase HPLC (acetonitrile/water, 0.05% TFA) to afford the title compound (12 mg, 0.02 mmol, 43%). MS (ESI): m/z 468 [M+H]+, 490 [M+Na]+. HPLC (reversed-phase): RT=9.71 min (single peak). 1H NMR (400 MHz, CDCl3): (rotameric broadening) 9.15 (s, 1H), 8.26 (dd, J=7.0 Hz, 1.0 Hz, 1H), 8.22 (dd, J=8.8 Hz, 1.0 Hz, 1H), 7.74 (d, J=2.1 Hz, 1H), 7.67 (dd, J=8.8 Hz, 7 Hz, 1H), 7.10 (d, J=8.3 Hz, 1H), 7.05 (m, 3H), 6.35 (t, J=2.2 Hz, 2H), 3.23 (bs, 4H), 1.61 (m, 2H), 1.48 (bs, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07550492B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-f65b6f6a53514357bc7a937467ac84e5 |
|---|
| Source note | uspto-grants-2009_06 |
|---|