Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 59152933 | HCID 59152933 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 44610986 | HCID 44610986 | 48.5% |
Reaction Steps
{(R)-4-[(3-Fluoro-5-trifluoromethyl-benzenesulfonyl)-methyl-amino]-4,5,6,7-tetrahydro-indazol-1-yl}-acetic acid (25 mg, 0.066 mmol) and pyrrolidine (47 mg, 0.66 mmol) were dissolved in dimethyl sulfoxide (1.5 mL). The mixture was heated in a microwave oven at 180° C. for 50 minutes. The resulting mixture was acidified with acetic acid to pH 4, and then filtered and purified by preparative HPLC to afford {(R)-4-[methyl-(3-pyrrolidin-1-yl-5-trifluoromethyl-benzenesulfonyl)-amino]-4,5,6,7-tetrahydro-indazol-1-yl}-acetic acid (15 mg, 48.5%) as a white powder. 1H NMR (400 MHz, CD3OD) δ ppm 7.24 (s, 1 H), 7.14 (s, 1 H), 6.98 (s, 1 H), 6.41 (s, 1 H), 5.05 (t, 1 H), 4.75 (s, 2 H), 3.35 (t, 4 H), 2.61 (s, 3 H), 2.45 (m, 2 H), 2.08-1.61 (m, 8 H). MS calcd. for C21H25F3N4O4S 486, obsd. (ESI+) [(M+H)+] 487.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124641B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-a1bdbec622194ba9ae1ebe931141181b |
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| Source note | uspto-grants-2012_02 |
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