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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912576Generated: November 3, 2026

2-Fluoro-6-methoxybenzyl bromide → HCID 71209476, compound

https://huagongshe.com/reaction/1912576

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-6-methoxybenzyl bromideHCID 2779322—
Reactantmethyl 2-(tert-butoxy)-2-(4-(chroman-6-yl)-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetateHCID 71209024—
ProductHCID 71209476HCID 71209476—

Reaction Steps

The title compound was prepared in a manner similar to that described in Example 27, Step H from methyl 2-(tert-butoxy)-2-(4-(chroman-6-yl)-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate and 2-fluoro-6-methoxybenzyl bromide. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.48-7.40 (m, 1 H), 7.32-7.28 (m, 1 H), 7.26-7.17 (m, 1 H), 7.04-6.99 (m, 1 H), 6.90 (dd, J=6.3, 8.3 Hz, 1 H), 6.78-6.69 (m, 2 H), 6.16-6.09 (m, 1 H), 5.62-5.55 (m, 2 H), 5.50-5.42 (m, 1 H), 4.30-4.24 (m, 2 H), 3.83 (d, J=1.8 Hz, 3 H), 2.94-2.78 (m, 2 H), 2.78-2.71 (m, 3 H), 2.07-2.03 (m, 2 H), 1.01-0.93 (s, 9 H); LC/MS (m/z) ES+=533.37 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609653B2
Source datasetuspto-grants-2013_12
ORD IDord-b8a99920a98a4c01b4fa4f42c07715a4
Source noteuspto-grants-2013_12