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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432922Generated: November 3, 2026

Bromoacetic Acid → 2-Benzyloxycarbonylamino-3-(bromoactyl-prop-2-ynyl-amino)-propionic acid methyl ester

https://huagongshe.com/reaction/1432922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetic AcidHCID 6227—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl esterHCID 54423640—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-Benzyloxycarbonylamino-3-(bromoactyl-prop-2-ynyl-amino)-propionic acid methyl esterHCID 13172772447.9%

Reaction Steps

DCC (2.27 g, 11.0 mmol) and bromoacetic acid (1.48 g, 10.7 mmol) is added to a solution of 2-benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester (3.10 g, 10.7 mmol) in CH2Cl2 at RT. The mixture is stirred overnight then diluted with ether. The white solid which precipitates out is filtered and the filtrate is concentrated to give a yellow oil. The crude product is purified by chromatography eluting with a gradient of 40% EtOAc/hexanes to 50% EtOAc/hexanes to yield the title product (2.1 g, 5.12 mmol) as an oil. 1H NMR (CDCl3, 300 MHz) δ7.30 (m, 5H), 5.70 (d, 1H), 5.10 (s, 2H), 4.63 (m, 1H), 4.15 (d, 2H), 4.00 (m, 1H), 3.80 (s, 3H), 3.75 (s, 2H), 3.70 (dd, 1H), 2.27 (bs, 1H). Ion spray MS, [M+H]+=411, 413, Br pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-356294f83e544092bde454bc39068ad5
Source noteuspto-grants-2009_11