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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099408Generated: October 27, 2026

(S)-N,N-dibenzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chroman-3-amine → HCID 25114919, compound

https://huagongshe.com/reaction/1099408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-N,N-dibenzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chroman-3-amineHCID 25114260—
Reactant5-bromo-2-methoxy-N-methylnicotinamideHCID 25114918—
ProductHCID 25114919HCID 2511491966%

Reaction Steps

The title compound was synthesized as described for Intermediate I-28 in 66% yield starting from (3S)-N,N-dibenzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)chroman -3-amine and 5-bromo-2-methoxy-N-methylnicotinamide; 1H NMR (400 MHz, DMSO-d6) δ ppm 8.33 (q, 1 H), 8.29 (d, 1 H), 8.06 (d, 1 H), 7.24-7.32 (m, 8 H), 7.11-7.21 (m, 3 H), 6.71-6.82 (m, 2 H), 4.26-4.38 (m, 1 H), 4.04 (s, 3 H), 4.01-4.11 (m, 1 H), 3.57-3.73 (m, 4 H), 2.87-3.09 (m, 2 H), 2.84 (d, 3 H), 2.46-2.54 (m, 1 H, obscured by DMSO); MS (ESI) m/z 494[M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143408B2
Source datasetuspto-grants-2012_03
ORD IDord-469dad0befcb444d8cef0f0a0d65974b
Source noteuspto-grants-2012_03