HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047915Generated: November 4, 2026
Methanol → 2-(Isoquinolin-5-ylcarbamoyl)-indan-2-carboxylic Acid
https://huagongshe.com/reaction/1047915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59314243 | HCID 59314243 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 2-(Isoquinolin-5-ylcarbamoyl)-indan-2-carboxylic Acid | HCID 59314087 | 86% |
Reaction Steps
A 30 mL reaction vial is charged with 2-(isoquinolin-5-ylcarbamoyl)-indan-2-carboxylic acid ethyl ester (320, 354 mg, 0.98 mmol) is charged with 1,4-dioxane (6 mL) and MeOH (6 mL). A stirring bar is added and stirring is initiated. After dissolution, water (3 mL) is added followed by the LiOH monohydrate (104 mg, 252 mmol). After 20 h, tlc analysis (silica, 10% MeOH/DCM) indicates that the starting material is completely consumed. Amberlyst highly acidic exchange resin (1 g) is added to the reaction vial. The reaction is capped and allowed to stir at ambient temperature. After 64 h, the contents of the flask are filtered through a pad of Celite. The solvent is removed from the filtrate by pumping to constant weight to give 0.29 g of off white solid. This material is triturated with DCM (15 mL). The solids are collected by suction filtration and washed with DCM (20 mL). Suction drying provides off white solid (280 mg, 86%).
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-cf11f05bdab0465482d707fca75fe9d1 |
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| Source note | uspto-grants-2013_10 |
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