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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661008Generated: October 27, 2026

Methyl 3-aminopropanoate hydrochloride → (+/-)-3-({5-[1-(4'-Tert-butyl-2,6-dimethyl-biphenyl-4-ylsulfanyl)-ethyl]-thiophene-2-carbonyl}-amino)-propionic acid methyl ester

https://huagongshe.com/reaction/661008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-aminopropanoate hydrochlorideHCID 2734767—
ReactantEthyl 5-(1-hydroxyethyl)thiophene-2-carboxylateHCID 59355961—
Reactant4'-tert-Butyl-2,6-dimethyl-biphenyl-4-thiolHCID 59356048—
Product(+/-)-3-({5-[1-(4'-Tert-butyl-2,6-dimethyl-biphenyl-4-ylsulfanyl)-ethyl]-thiophene-2-carbonyl}-amino)-propionic acid methyl esterHCID 59355959—

Reaction Steps

This compound is made by the general method as exemplified in Preparation 107 using 4′-tert-butyl-2,6-dimethyl-biphenyl-4-thiol and (±)-5-(1-hydroxy-ethyl)-thiophene-2-carboxylic acid ethyl ester in Step A and 3-amino-propionic acid methyl ester hydrochloride salt in Step C as the starting materials to provide (±)-3-({5-[1-(4′-tert-butyl-2,6-dimethyl-biphenyl-4-ylsulfanyl)-ethyl]-thiophene-2-carbonyl}-amino)-propionic acid methyl ester (0.279 g) as a white foam. MS (ES): 508.3 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084489B2
Source datasetuspto-grants-2011_12
ORD IDord-e7e92d75e805418b9382ee03f64ea169
Source noteuspto-grants-2011_12