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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913931Generated: November 4, 2026

HCID 57546116, compound → HCID 57546213, compound

https://huagongshe.com/reaction/913931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57546116HCID 57546116—
ReactantHCID 57546152HCID 57546152—
ProductHCID 57546213HCID 57546213—

Reaction Steps

Prepared according to the procedure used to prepare tert-butyl 4-((1-(5-chloro-1H-indazol-7-yl)-2-methoxy-2-oxoethoxy)methyl)-4-(4-fluorophenyl)piperidine-1-carboxylate using tert-butyl 4-(((5-chloro-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-7-yl)(cyano)methoxy)methyl)-4-(4-fluorophenyl)piperidine-1-carboxylate as the starting material. 1H-NMR (CDCl3, 500 MHz) δ 9.66 (bs, 1H), 7.98 (s, 1H), 7.74 (d, J=1.5 Hz, 1H), 7.31 (m, 3H), 7.13 (dd, J=8.6, 8.6 Hz, 2H), 5.46 (s, 1H), 3.60-3.90 (m, 4H), 3.07 (m, 2H), 2.18 (m, 2H), 1.82 (m, 2H), 1.43 (s, 9H); 13C NMR (126 MHz, CDCl3) δ ppm 171.2, 161.9 (d, J=248 Hz), 154.9, 137.4, 135.6, 134.4, 128.6 (d, J=7.7 Hz), 126.3, 125.5, 125.4, 122.0, 116.2 (d, J=21 Hz), 79.9, 78.9, 69.5, 41.1, 39.9 (br), 32.5, 32.3, 28.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026257B2
Source datasetuspto-grants-2011_09
ORD IDord-7cf8db3fb05044b296f2a659dfadff4e
Source noteuspto-grants-2011_09