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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276801Generated: October 31, 2026

HCID 71571988, compound → HCID 71525317, compound

https://huagongshe.com/reaction/2276801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71571988HCID 71571988—
ReactantHCID 178421689HCID 178421689—
ProductHCID 71525317HCID 71525317—
ProductHCID 178421689HCID 178421689—

Reaction Steps

(R)-2-(4-(4-chloro-2-fluorophenoxy)phenyl)-6-(1,2-dihydroxyethyl) pyrimidine-4-carboxamide (Compound Example No. 9) was prepared in a similar fashion to (R)-2-(4-(5-chloro-2-fluorophenoxy)phenyl)-6-(1,2-dihydroxyethyl) pyrimidine-4-carboxamide (Compound Example No. 7) using 2-(4-(4-chloro-2-fluorophenoxy)phenyl)-4,4,5,5-tetramethyl-1,3,3-dioxaborolane (6) instead of 2-(4-(5-chloro-2-fluorophenoxy)phenyl)-4,4,5,5-tetramethyl-1,3,3-dioxaborolane (14). 1H NMR (400 MHz, CD3OD): 8.49 (2H, d, J=8.8 Hz), 8.03 (1H, s), 7.30 (1H, dd, J=2.8, 10 Hz), 7.18-7.10 (2H, m), 6.96 (2H, d, J=9.2 Hz), 4.73 (1H, dd, J=3.2, 5.6 Hz), 3.89 (1H, dd, J=3.6, 11 Hz), 3.75 (1H, dd, J=6.0, 11 Hz); LC/MS: m/z=404[M+H]+. Compound 6 was prepared according to Scheme 1 in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133131B2
Source datasetuspto-grants-2015_09
ORD IDord-27147c7dffa444e388a5496b99b6cecf
Source noteuspto-grants-2015_09