HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865862Generated: October 26, 2026
Dimethylformamide → (S)-2-(3-Benzothiazol-6-yl-phenylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1865862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 6-Bromo-1,3-benzothiazole | HCID 2795171 | — |
| Reactant | (S)-2-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester | HCID 24828649 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | (S)-2-(3-Benzothiazol-6-yl-phenylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester | HCID 57977832 | — |
Reaction Steps
A solution of (S)-2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester (74 mg, 0.16 mmol), 6-bromo-benzothiazole (34.9 mg, 0.16 mmol), and Pd[P(Ph)3]4 (12.1 mg, 6.4 mol %) in methanol (2 mL), NaHCO3 (sat. aq., 300 μL), and DMF (400 μL) was degassed and heated to 70° C. overnight in a sealed vial. The reaction was cooled, filtered, and purified by reverse phase HPLC to give the desired product. Yield 5.6 mg. MS: 458.1 (M+H+); H1 NMR (DMSO-d6): δ (ppm) 1.18-1.25 (m, 2H), 1.76-2.00 (m, 3H), 2.10-2.34 (m, 1H), 4.28-4.40 (m, 1H), 4.87-5.10 (m, 2H), 7.00-7.56 (m, 7H), 7.68-7.66 (m, 1H), 7.97-8.15 (m, 2H), 8.33-8.39 (m, 1H), 9.35-9.39 (s, 1H), 10.09-10.16 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629340B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-7681da30217f4731bdc5b07bbd98c182 |
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| Source note | uspto-grants-2009_12 |
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