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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428973Generated: October 31, 2026

HCID 57413724, compound → HCID 57413591, compound

https://huagongshe.com/reaction/1428973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57413724HCID 57413724—
ReactantHCID 57413864HCID 57413864—
ReactantHCID 86674310HCID 86674310—
ProductHCID 57413591HCID 5741359169%

Reaction Steps

Using the procedure outlined in the synthesis of 5b with [(2R,3S,4S,5R,6R)-4,5-diacetoxy-6-(acetoxymethyl)-2-(4-bromo-2-trifluoromethyl-phenoxy)tetrahydropyran-3-yl]acetate (0.57 g) and N1,N3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-dicarboxamide (9) (0.48 g), the title compound was obtained (0.340 g) in 69% yield for the two steps. 1H NMR (300 MHz, METHANOL-d4) δ ppm 8.17-8.24 (m, 1H), 8.14 (d, J=1.65 Hz, 2H), 7.92 (d, J=1.92 Hz, 1H), 7.87 (dd, J=2.20, 8.79 Hz, 1H), 7.57 (d, J=8.79 Hz, 1H), 5.64 (d, J=1.65 Hz, 1H), 4.04 (dd, J=1.65, 3.30 Hz, 1H), 3.87-3.96 (dd, 1H), 3.64-3.83 (m, 3H), 3.48-3.63 (m, 1H), 2.93 (s, 6H). MS (ESI): found: [M+H]+, 515.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937167B2
Source datasetuspto-grants-2015_01
ORD IDord-bfbdb7dd8e384ce7a10d6a180b622a26
Source noteuspto-grants-2015_01