Hydrochloric Acid → 4-(6-Cyano-4-(methoxycarbonyl)chroman-7-yloxy)-3-methylbenzoic acid

HRID 510721Notes

Reaction equation

C([O-])([O-])=O.[K+].[K+].[C:7]([C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1F)[O:15][CH2:14][CH2:13][CH:12]2[C:20]([O:22][CH3:23])=[O:21])#[N:8].[OH:24][C:25]1[CH:37]=[CH:36][C:28]([C:29]([O:31]C(C)(C)C)=[O:30])=[CH:27][C:26]=1[CH3:38].Cl>CN1C(=O)CCC1>[C:7]([C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[O:24][C:25]1[CH:37]=[CH:36][C:28]([C:29]([OH:31])=[O:30])=[CH:27][C:26]=1[CH3:38])[O:15][CH2:14][CH2:13][CH:12]2[C:20]([O:22][CH3:23])=[O:21])#[N:8]

Participants

Conditions

Temperature: 120 °C

Procedure

A mixture of K2CO3 (0.026 g, 0.19 mmol), methyl 6-cyano-7-fluoro-3,4-dihydro-2H-chromene-4-carboxylate (0.040 g, 0.17 mmol), and tert-butyl 4-hydroxy-3-methylbenzoate (0.039 g, 0.19 mmol) in 0.5 ml NMP was heated under argon at 120° C. for 24 hours. The reaction was cooled, poured into 10% aqueous HCl, and extracted with ethyl acetate. The organic extracts were dried with sodium sulfate and purified on silica gel. Elution with 25% ethyl acetate-hexanes provided material that still contained impurities. The mixture was deprotected with to 1:1 trifluoracetic acid-dichloromethane to provide the title compound (13 mg, still impure) which was used directly in the next step.

Workup

temperatureThe reaction was cooled
extractionextracted with ethyl acetate
dry with materialThe organic extracts were dried with sodium sulfate
custompurified on silica gel
washElution with 25% ethyl acetate-hexanes provided material that still contained impurities

Sources & evidence

ORD record: ord-65068cbdd5b244b1acc45d4eda63b732
Source dataset: uspto-grants-2015_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09096567B2

Reaction notes

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