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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422636Generated: October 26, 2026

{(S)-6-[(R)-4-Bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester → {(S)-6-[(R)-4-(7,8-Dihydro-pyrido[4,3-d]pyrimidin-6-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

https://huagongshe.com/reaction/1422636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{(S)-6-[(R)-4-Bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 86700813—
Reactant(7,8-Dihydro-pyrido[4,3-d]pyrimidin-6-yl)methyltrifluoroborateHCID 131732226—
Product{(S)-6-[(R)-4-(7,8-Dihydro-pyrido[4,3-d]pyrimidin-6-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 90313477—

Reaction Steps

The title compound is prepared from {(S)-6-[(R)-4-bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and (7,8-dihydro-pyrido[4,3-d]pyrimidin-6-yl)methyltrifluoroborate following a procedure analogous to that described for Intermediate 3. LC (method 1): tR=1.13 min; Mass spectrum (ESI+): m/z=540 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927531B2
Source datasetuspto-grants-2015_01
ORD IDord-484b3f66e95a48c8ae44604e92623a6d
Source noteuspto-grants-2015_01