HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620286Generated: October 25, 2026
Lithium Hydroxide → HCID 178486611, compound
https://huagongshe.com/reaction/1620286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 3-(Chloromethyl)quinoline hydrochloride | HCID 14548126 | — |
| Reactant | 3-(chloromethyl)-6-methoxy-N-(2-methoxyethyl)quinolin-2-amine hydrochloride | HCID 68182273 | — |
| Reactant | HCID 178486705 | HCID 178486705 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178486611 | HCID 178486611 | — |
Reaction Steps
To a solution of 1-isopropyl-6,7-dimethoxyisoquinolin-3-ol SIL 32164 (462 mg, 1.87 mmol) in THF (13 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added a 3-(chloromethyl)quinoline hydrochloride SLA 47064B (400 mg, 1.87 mmol) and a 2 N aq. LiOH solution (1.87 mL, 3.74 mmol) and the mixture was stirred at 160° C. for 1.5 h under microwave irradiation. After cooling to RT, THF was removed at 40° C. under vacuum and the residue was taken up in CH2Cl2 (50 mL), washed with brine (10 mL), dried over Na2SO4, filtered, and concentrated under vacuum. Purification by column chromatography (SiO2, eluent CH2Cl2:MeOH=100:0 to 94:6) provided 1-isopropyl-6,7-dimethoxy-4-(quinolin-3-ylmethyl)isoquinolin-3-ol. This free base was dissolved in MeOH (2 mL) in a 10 mL round-bottomed flask equipped with a magnetic stirrer before addition of 0.149 M HCl solution in MeOH (2.0 mL). The reaction mixture was stirred for 5 min at RT and concentrated at 40° C. under vacuum to afford 1-isopropyl-6,7-dimethoxy-4-(quinolin-3-ylmethyl)isoquinolin-3-ol dihydrochloride 79 as a yellow solid (76 mg, 9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772316B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-0428c531871c4da9b31a3537fd031a6c |
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| Source note | uspto-grants-2014_07 |
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