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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283402Generated: October 30, 2026

HCID 89544762, compound → HCID 89544746, compound

https://huagongshe.com/reaction/2283402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 89544762HCID 89544762—
ReactantHCID 131733519HCID 131733519—
ProductHCID 89544746HCID 89544746—

Reaction Steps

Step 2 ((R)-1-{3-[4-(tert-Butyl-dimethyl-silanyloxymethyl)-benzoyl]-4-chloro-2-fluoro-phenyl}-propyl)-carbamic acid tert-butyl ester was deprotected as Step 2 in the preparation of Example 2. A mixture of the doubly deprotected product [3-((R)-1-amino-propyl)-6-chloro-2-fluoro-phenyl]-(4-hydroxymethyl-phenyl)-methanone (=Example 50) and the trans-esterified product acetic acid 4-[3-((R)-1-amino-propyl)-6-chloro-2-fluoro-benzoyl]-benzyl ester (=Example 49) was obtained. Separation was achieved by column chromatography with 0-8% ammonia in methanol/dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145354B2
Source datasetuspto-grants-2015_09
ORD IDord-ad7fa68ca2934e549743ef958a6a93ea
Source noteuspto-grants-2015_09