HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172529Generated: November 2, 2026
Cyclopropylamine → 4-Chloro-2-(2-cyclopropylamino-acetylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester
https://huagongshe.com/reaction/1172529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 4-Chloro-2-(2-chloro-acetylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester | HCID 11633641 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-2-(2-cyclopropylamino-acetylamino)-6-methyl-10,10-dioxo-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester | HCID 131728498 | — |
Reaction Steps
Cyclopropyl amine (0.285 ml, 4.067 mmol) was added to a solution of Example 133 (0.6 g, 1.35 mmol) in DMF (15 mL) and the reaction mixture was stirred at 80° C. for 2 h. It was concentrated, treated with water and the solid that precipitated was filtered, washed with water and purified using flash chromatography (silica gel, 2% methanol/chloroform) to obtain the title compound as a white solid. Yield: 0.58 g (92%); 1H NMR (CDCl3): δ 0.6 (s, 4H, 2CH2), 2.4 (m, 1H, CH), 2.67 (s, 3H, CH3), 3.6 (s, 2H, CH2), 3.9 (s, 3H, OCH3), 4.7 (s, 2H, CH2), 7.6 (s, 1H, Ar), 7.65 (s, 1H, Ar), 8.1 (s, 1H, Ar), 8.45 (s, 1H, Ar), 9.35 (bs, 1H, NH); MS: m/e (ES+) 465 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834001B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-5b98088271a64a6eac3e14adb34afc02 |
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| Source note | uspto-grants-2010_11 |
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