HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645346Generated: October 25, 2026
2,2-Dimethylsuccinic anhydride → 4-(4-{5-[(4-Chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid
https://huagongshe.com/reaction/1645346
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Dimethylsuccinic anhydride | HCID 87067 | — |
| Reactant | 4-Chloro-benzo[b]thiophene-2-carboxylic acid (6-piperazin-1-yl-pyridin-3-yl)-amide | HCID 59365178 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-{5-[(4-Chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid | HCID 46207828 | 89.1% |
Reaction Steps
A mixture of 4-chloro-benzo[b]thiophene-2-carboxylic acid (6-piperazin-1-yl-pyridin-3-yl)-amide (50 mg, 0.13 mmol), CH2Cl2 (5 mL), and TEA (40 mg, 0.39 mmol) was stirred at room temperature. 2,2-Dimethylsuccinic anhydride (36 mg, 0.28 mmol) was added slowly. The reaction was stirred at room temperature for 0.5 hr then concentrated and the residue was taken up into 50 mL of EtOAc and washed with 50 mL of saturated ammonium chloride, brine and dried over anhydrous sodium sulfate. The solvent was removed and the product was triturated with diethyl ether and hexanes followed by filtration, to afford the product 4-(4-{5-[(4-chloro-benzo[b]thiophene-2-carbonyl)-amino]-pyridin-2-yl}-piperazin-1-yl)-2,2-dimethyl-4-oxo-butyric acid (58 mg, 89% yield). LCMS for C24H25ClN4O4S calcd. (m/e) 500, observed 499 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124766B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-851927c92ab04157a1b7523151f01bd0 |
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| Source note | uspto-grants-2012_02 |
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