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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292892Generated: October 31, 2026

2-Methylphenyl boronic acid → tert-butyl(6aS,10aR)-2-(2-methylphenyl)-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)-carboxylate

https://huagongshe.com/reaction/1292892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylphenyl boronic acidHCID 2733267—
ReactantTert-butyl (6aS,10aR)-2-bromo-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)carboxylateHCID 20577007—
Producttert-butyl(6aS,10aR)-2-(2-methylphenyl)-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)-carboxylateHCID 10453012—

Reaction Steps

The title compound was prepared by the method of Example 89 step C from tert-butyl (6aS,10aR)-2-bromo-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH) carboxylate (189 mg, 0.5 mmol) and 2-methylphenylboronic acid (136 mg, 1.0 mmol) to afford after chromatographic purification the title compound (90 mg, 46%). 1H NMR (CDCl3, 300 MHz) δ 7.11-7.18 (m,4H), 6.82 (s, 1H), 6.77 (s, 1H), 3.86-4.30 (m, 2H), 3.58-3.64 (m, 1H), 2.76-3.42 (m, 7H), 2.20 (s, 3H), 1.70-1.85 (m, 2H), 1.40 (s, 9H) ppm. MS-ApCI: 391 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238690B2
Source datasetuspto-grants-2007_07
ORD IDord-ed8067d971ed42cbba34741656600e5a
Source noteuspto-grants-2007_07