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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593848Generated: October 31, 2026

N-Boc-4-chloro-D-phenylalanine → 4-Chloro-D-phenylalanine methyl ester hydrochloride

https://huagongshe.com/reaction/1593848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Boc-4-chloro-D-phenylalanineHCID 7018791—
Reactant(R)-2-[2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4,5-dichloro-benzoylamino]-3-(4-chloro-phenyl)-propionic acidHCID 11671504—
Product4-Chloro-D-phenylalanine methyl ester hydrochlorideHCID 24720899—

Reaction Steps

(R)-2-[2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4,5-dichloro-benzoylamino]-3-(4-chloro-phenyl)-propionic acid. (R)-2-(tert-Butoxycarbonylamino)-3-(4-chloro-phenyl)-propionic acid was treated as in EXAMPLE 2, Part A, to produce (R)-2-amino-3-(4-chloro-phenyl)-propionic acid methyl ester hydrochloride as a white solid. This salt was then coupled with 2-(benzo[1,2,5]thiadiazole-4-sulfonylamino)-4,5-dichloro-benzoic acid as in EXAMPLE 1, Part C. The resulting methyl ester was hydrolyzed as in EXAMPLE 2, Part E, to afford the title compound. HPLC: RT=10.35 min. MS (ESI−): mass calcd. for C22H15Cl3N4O5S2, 583.95; m/z found, 583/585 [M−H]−. 1H NMR (500 MHz, CDCl3): 11.07 (s, 1H), 8.34 (d, J=7.1, 1H), 8.23 (d, J=8.8, 1H), 7.84 (s, 1H), 7.74-7.70 (m, 1H), 7.30-7.26 (m, 2H), 7.24 (s, 1H), 7.07 (d, J=8.3, 2H), 6.38 (d, J=7.4, 1H), 5.00-4.97 (m, 1H), 3.30 (dd, J=14.1, 5.9, 1H), 3.21 (dd, J=14.1, 5.9, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297816B2
Source datasetuspto-grants-2007_11
ORD IDord-897b41202d5e4fa1945bba3db6aad1a9
Source noteuspto-grants-2007_11