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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389594Generated: November 1, 2026

HCID 66697928, compound → HCID 66760644, compound

https://huagongshe.com/reaction/389594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66697928HCID 66697928—
ReactantHCID 66759397HCID 66759397—
ProductHCID 66760644HCID 667606443%

Reaction Steps

The title compound was prepared in 3% yield from 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phthalazine and 1-{4-[4-(7-amino-2-chlorofuro[2,3-c]pyridin-4-yl)-1H-pyrazol-1-yl]piperidin-1-yl}ethanone, by a procedure analogous to Example 223, Step D. The sample underwent both mass-directed purification and preparative TLC during purification. 1H NMR (400 MHz, CD3OD): δ 10.32 (s, 1H), 9.73 (s, 1H), 8.63 (dd, J=0.76, 7.58 Hz, 1H), 8.32 (d, J=8.08 Hz, 1H), 8.18-8.25 (m, 2H), 7.96-8.03 (m, 2H), 7.76 (s, 1H), 4.67-4.76 (m, 1H), 4.55-4.61 (m, 1H), 3.35-3.42 (m, 1H), 2.88 (dt, J=2.65, 12.95 Hz, 1H), 2.21-2.31 (m, 2H), 2.19 (s, 3H), 1.98-2.18 (m, 3H); MS (ESI): 454.19 [M+H]+; HPLC tR=0.85 min (TOF: polar—3 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-b8fd8ade4f1f4b02a59cd14f4ec562ad
Source noteuspto-grants-2013_02