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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432121Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 59118110, compound

https://huagongshe.com/reaction/432121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 4-[(2R)-2-[((tert-butoxycarbonyl)[(2R)-2-{[tert-butyl(dimethyl)silyl]-oxy}-2-[6-(2,5-dimethyl-1H-pyrrol-1-yl)-3-pyridinyl]ethyl}amino)methyl]-3,4-dihydro-2H-chromen-6-yl}benzoateHCID 59118169—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59118110HCID 59118110120.1%

Reaction Steps

To a solution of methyl 4-{(2R)-2-[((tert-butoxycarbonyl){(2R)-2-{[tert-butyl(dimethyl)silyl]-oxy}-2-[6-(2, 5-dimethyl-1H-pyrrol-1-yl)-3-pyridinyl]ethyl}-amino)methyl]-3,4-dihydro-2H-chromen-6-yl}benzoate (Example 371, 213 mg, 0.29 mmol) in THF (5 mL) was added a solution of 1 M tetrabutylammonium fluoride (0.59 mL, 0.59 mmol). The mixture was stirred at room temperature for 16 hours and then concentrated in vacuo. Flash chromatography of the residue over silica gel using 40% ethyl acetate/hexanes afforded 213 mg (92%) of the desired product. The product had: 1H NMR (CDCl3δ): 8.62 (s, 1H), 8.06 (d, J=8.9 Hz, 2H), 7.92 (d, J=7.2 Hz, 1H), 7.58 (d, J=8.8 Hz, 2H), 7.31-7.40 (m, 2H), 7.22 (d, J=7.8 Hz, 1H), 6.89 (d, J=7.9 Hz, 1H), 5.89 (s, 2H), 5.10-5.26 (m, 2H), 4.21-4.50 (m, 1H), 3.93 (s, 3H), 3.56-3.88 (m, 4H), 3.15-3.42 (m, 1H), 2.78-3.04 (m, 2H), 2.12 (s, 6H), 1.65-1.83 (m, 2H), 1.50 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660752B2
Source datasetuspto-grants-2003_12
ORD IDord-d427d8ea49f74cdb957d3fa94e83df89
Source noteuspto-grants-2003_12