HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047933Generated: October 27, 2026
Dichloromethane → 2-[(2,5-Dichloro-pyridine-3-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1047933
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,5-Dichloro-nicotinoyl chloride | HCID 2799996 | — |
| Reactant | Ethyl 2-amino-2,3-dihydro-1H-indene-2-carboxylate | HCID 10921653 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Isopropanol methylene chloride | HCID 21966342 | — |
| Product | 2-[(2,5-Dichloro-pyridine-3-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester | HCID 59314226 | 107.7% |
Reaction Steps
A 30 mL reaction vial is charged with 2-aminoindan-2-carboxylic acid ethyl ester (1 g, 4.87 mmol) and dry DCM (5 mL). A stirring bar is added and stirring is initiated. DIPEA (1.35 mL, 7.8 mmol) is added. 2,5-dichloro-pyridine-3-carbonyl chloride (1.23 g, 5.85 mmol) and DMAP (8 mg, cat.) are added. The reaction is capped. After 57 days, tlc analysis (silica, 10% iPrOH/DCM) indicates that the starting has been completely consumed. The contents of the reaction flask are transferred to a separatory funnel and diluted with EtOAc (60 mL). This is washed with water (2×25 mL), saturated aqueous NaHCO3 (2×25 mL), and brine (25 mL), and then dried over MgSO4, filtered and evaporated by pumping to constant weight yields 1.99 g of off-white solid. This is diluted with DCM (20 mL) and applied to a silica column ((80 g) on an ISCO Companion. The column is eluted with 5% EtOAc in heptanes for 3 column volumes followed by a linear gradient to 75% EtOAc in heptanes over 12 column volumes. 17 mL fractions of UV positive eluent are collected. Fraction 12-16 are combined and evaporated by pumping to constant weight to give light yellow solid (1.39 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569535B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-404fd16f4dcd45a999ce204fb9428988 |
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| Source note | uspto-grants-2013_10 |
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