HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-chloro-L-phenylalanine → HCID 67516744, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-chloro-L-phenylalanine | HCID 2761492 | — |
| Reactant | (3R,4S)-3-amino-4-(3-boronopropyl)-1-((6-chloro-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl)pyrrolidine-3-carboxylic acid trihydrochloride | HCID 67516743 | — |
| Product | HCID 67516744 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09233985B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-0c5f0edf75db44c99286579cc9c18b8a |
| Source note | uspto-grants-2016_01 |