HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551098Generated: October 31, 2026
1,2-Dichloroethane → HCID 16112824, compound
https://huagongshe.com/reaction/551098
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57663771 | HCID 57663771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 16112824 | HCID 16112824 | — |
Reaction Steps
A mixture of [4-oxo-1-{[(7S)-2′-oxo-1′,2′,6,8-tetrahydrospiro[cyclopenta[g]quinoline-7,3′-pyrrolo[2,3-b]pyridin]-2-yl]methyl}-1,2,4,5-tetrahydropyrrolo[4,3,2-de]quinolin-2a(3H)-yl]acetic acid, diastereomer A (50 mg, 0.094 mmol, described in Example 2), pyrrolidine (20 mg, 0.282 mmol), EDC (22 mg, 0.113 mmol), HOBT (17 mg, 0.113 mmol), and N,N-diisopropylethylamine (0.082 mL, 0.470 mmol) was stirred in DMF (0.5 mL) at ambient temperature for 18 h. The reaction mixture was partitioned between saturated aqueous NaHCO3 (20 mL) and CH2Cl2 (10 mL). The organic layer was removed and the aqueous layer was extracted further with CH2Cl2 (2×10 mL). The combined organic extracts were washed with brine (10 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 95:5, to give the title compound. MS: m/z=585 (M+1). HRMS: m/z=585.2620; calculated m/z=585.2609 for C35H33N6O3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947677B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-28c9046e512d4b039d90b8a591d98500 |
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| Source note | uspto-grants-2011_05 |
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