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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716968Generated: November 1, 2026

Triethylamine → HCID 59013438, compound

https://huagongshe.com/reaction/1716968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-ChlorodimethylamineHCID 123122—
ReactantHCID 86616575HCID 86616575—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59013438HCID 5901343852%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ((1S,3′R,4′S,5′S,6′R)-5-chloro-6-(4-iso-propylbenzyl)-3′,4′,5′-trihydroxy-3′,4′,5′,6′-tetrahydro-3H-spiro[isobenzofuran-1,2′-pyran]-6′-yl)methyl 4-methylbenzenesulfonate (15 mg, 0.025 mmol) and dimethylamino hydrochloride (48 mg, 0.588 mmol) in DMF (1 mL), was added Et3N (67 mg, 0.662 mmol). After being stirred for 24 h at 80° C., the reaction mixture was diluted with H2O and extracted 3× with AcOEt. The combined organic layers were washed with brine prior to drying over Na2SO4. The volatiles were removed under reduced pressure. The resulting residue was purified by preparative HPLC to yield 6 mg of title compound. 1H NMR (CD3OD, 300 MHz) δ 7.41 (s, 1H), 7.24 (s, 1H), 7.13 (s, 4H), 5.18 (d, J=13.5 Hz, 1H), 5.13 (d, J=13.5 Hz, 1H), 4.17-4.02 (m, 3H), 3.76-3.75 (m, 2H), 3.46-3.18 (m, 3H), 2.90-2.81 (m, 1H), 2.76 (s, 6H), 1.22 (d, J=6.9 Hz, 6H); MS ESI (m/z) 462 (M+1)+, calc. 461.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803778B2
Source datasetuspto-grants-2010_09
ORD IDord-7b48aab54f384083842f4f55f95d5a3a
Source noteuspto-grants-2010_09