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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678145Generated: November 1, 2026

2-chloro-1-phenyl-1H-indole-3-carbaldehyde → 4-(3-formyl-1-phenyl-1H-indole-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1678145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-1-phenyl-1H-indole-3-carbaldehydeHCID 314793—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
Product4-(3-formyl-1-phenyl-1H-indole-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl esterHCID 8659681087%

Reaction Steps

2-Chloro-1-phenyl-1H-indole-3-carboxaldehyde is reacted with [1,4]diazepane-1-carboxylic acid tert-butyl ester as described in Example 1 to afford 4-(3-formyl-1-phenyl-1H-indole-2-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (87% yield) as a yellow solid. LC/MS MS 420 (M+H); RT 3.55 min; NMR (CDCl3): 10.25 (1H, s), 8.27 (1 H, d), 7.46-7.66 (3H, m), 7.37 (2H, d), 7.22-7.30 (1H, t), 7.16(1 H, t), 6.96 (1 H, d), 3.25-3.45 (8H, m), 1.56 (2H, m), 1.44(9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008491B2
Source datasetuspto-grants-2011_08
ORD IDord-2e2f56bf0b2b4c299bf316189f670870
Source noteuspto-grants-2011_08