HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887800Generated: October 28, 2026
Diisopropylethylamine → HCID 71208954, compound
https://huagongshe.com/reaction/1887800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 2-Bromothiazole-5-carboxylic acid | HCID 2763210 | — |
| Reactant | 3-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one | HCID 71208398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71208954 | HCID 71208954 | 93.1% |
Reaction Steps
To a stirred solution of 2-bromothiazole-5-carboxylic acid (241 mg, 1.16 mmol) and N,N-diisopropylethylamine (409 mg, 552 μL, 3.16 mmol) in methylene chloride was added (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) (559 mg, 1.26 mmol). After 15 min., 3-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one (intermediate D) (300 mg, 1.05 mmol) was added. The reaction mixture was stirred at room temperature. The mixture was diluted with CH2Cl2 and washed with water followed by 1N aqueous HCl and finally saturated aqueous sodium carbonate solution. The organic layer was dried (Na2SO4), filtered and concentrated. The product 2-bromo-thiazole-5-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide (464 mg, 93%) was obtained without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501732B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-915f40b7f8a144e9bf13b5a35675f697 |
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| Source note | uspto-grants-2013_08 |
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