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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590746Generated: October 30, 2026

3-chloro-L-phenylalanine → HCID 67516744, compound

https://huagongshe.com/reaction/590746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-chloro-L-phenylalanineHCID 2761492—
Reactant(3R,4S)-3-amino-4-(3-boronopropyl)-1-((6-chloro-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl)pyrrolidine-3-carboxylic acid trihydrochlorideHCID 67516743—
ProductHCID 67516744HCID 67516744—

Reaction Steps

(3R,4S)-3-amino-4-(3-boronopropyl)-1-((6-chloro-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl)pyrrolidine-3-carboxylic acid trihydrochloride (mixture of two diastereomers, each a racemate) is prepared in a manner analogous to that set forth in Example 49, except 3-chlorophenylalanine is used in place of 4-chlorophenylalanine in Step 1. 1H NMR (0.1M DCl in D2O, 400 MHz) δ 7.23 (m, 2 H), 7.09 (m, 1 H), 4.37 (s, 2 H), 4.00 (m, 3 H), 3.82 (m, 2 H), 3.69 (m, 1 H), 3.43 (m, 1 H), 3.22 (m, 1 H), 3.00 (m, 1 H), 2.68 (m, 1 H), 1.60 (m, 1 H), 1.26 (m, 3 H), 0.66 (m, 2 H). ESI+ MS found for C18H27BClN3O4 m/z 378.1 (M−18+H), 360.0 (M−36+H); ESE MS m/z 376.1 (M−18−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233985B2
Source datasetuspto-grants-2016_01
ORD IDord-0c5f0edf75db44c99286579cc9c18b8a
Source noteuspto-grants-2016_01