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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920635Generated: October 27, 2026

3-Phenoxyphenylacetic acid → (S)-2-{(S)-3-(3,4-Dimethoxy-phenyl)-2-[2-(3-phenoxy-phenyl)-acetylamino]-propionylamino}-3-methyl-N-[(R)-3-methyl-1-((1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)-butyl]-butyramide

https://huagongshe.com/reaction/1920635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenoxyphenylacetic acidHCID 141749—
ReactantN-((1,1-Dimethylethoxy)carbonyl)-3-methoxy-O-methyl-L-tyrosineHCID 10829890—
Reactant{(S)-2-Methyl-1-[(R)-3-methyl-1-((1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)-butylcarbamoyl-]propyl}-carbamic acid tert-butyl esterHCID 67492646—
Product(S)-2-{(S)-3-(3,4-Dimethoxy-phenyl)-2-[2-(3-phenoxy-phenyl)-acetylamino]-propionylamino}-3-methyl-N-[(R)-3-methyl-1-((1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)-butyl]-butyramideHCID 10169507—

Reaction Steps

The title compound is prepared from {(S)-2-Methyl-1-[(R)-3-methyl-1-((1S,2S,6R,8S)-2,9,9-trimethyl-3,5-dioxa-4-bora-tricyclo[6.1.1.02,6]dec-4-yl)-butylcarbamoyl]-propyl}-carbamic acid tert-butyl ester by reiteration of the 2-step (deprotection/coupling) procedure described in example 1 but using Boc-L-3,4-dimethoxyphenylalanine (Synthetech) and (3-Phenoxy-phenyl)-acetic acid (Trans World Chemicals, Inc.; Rockville, Md., USA) as the partners in each coupling reaction (step B, example 1), respectively. The title compound is obtained as a foam; ES-MS: 782.3 [M+H]+; HPLC: single peak at tR=11.76 min (System 1); Rf=0.61 (CH2Cl2/MeOH, 90/10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173128B2
Source datasetuspto-grants-2012_05
ORD IDord-25e755a29fa7440aa0f0989b418c68b1
Source noteuspto-grants-2012_05