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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623010Generated: October 31, 2026

5-Tert-butylthiophene-2-carboxylic acid → tert-butyl (5-(tert-butyl)thiophene-2-carbonyl)-L-tyrosinate

https://huagongshe.com/reaction/1623010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Tert-butylthiophene-2-carboxylic acidHCID 458349—
ReactantL-Tyrosine 1,1-dimethylethyl esterHCID 6950582—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Producttert-butyl (5-(tert-butyl)thiophene-2-carbonyl)-L-tyrosinateHCID 8668967889.2%

Reaction Steps

Prepared using General Procedure 7. Into a solution of 5-(tert-butyl)thiophene-2-carboxylic acid (1.93 g, 10.0 mmol) in DMF (20 mL) were added HATU (4.56 g, 12.0 mmol) and TEA (4.18 mL, 30.0 mmol). The mixture was stirred at room temperature for 30 min and (S)-tert-butyl 2-amino-3-(4-hydroxyphenyl)propanoate (2.37 g, 10.0 mmol) was added. After 1 h, the reaction mixture was poured into 400 mL of ice-water and the solid was filtered. The solid was dissolved in DCM and EA, dried over MgSO4, concentrated, and purified by chromatography (EA/hexanes) to provide 3.6 g (89%) of tert-butyl (5-(tert-butyl)thiophene-2-carbonyl)-L-tyrosinate. LCMS-ESI (m/z) calculated for C22H29NO4S: 403.2; found: 426.1 [M+Na]+, tR=9.07 min (Method 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778923B2
Source datasetuspto-grants-2014_07
ORD IDord-d74c2aa41b564ae6aceeb57e81ec1ea2
Source noteuspto-grants-2014_07