Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422640Generated: November 2, 2026

5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazine → HCID 90314122, compound

https://huagongshe.com/reaction/1422640

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazineHCID 13247046—
Reactant{(S)-6-[(R)-4-Bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 86700813—
Reactant{(S)-6-[(R)-4-(5,6-dihydro-8H-imidazo[1,2-a]pyrazin-7-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 90314440—
ProductHCID 90314122HCID 90314122—

Reaction Steps

The methyl ester of the title compound, {(S)-6-[(R)-4-(5,6-dihydro-8H-imidazo[1,2-a]pyrazin-7-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester, is prepared from {(S)-6-[(R)-4-bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyrazine following a procedure analogous to that described for Intermediate 42. The crude product is directly submitted to the saponification conditions described for Example 1 to give the title compound upon chromatography on reversed phase (HPLC; acetonitrile/water). LC (method 6): tR=0.76 min; Mass spectrum (ESI+): m/z=514 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927531B2
Source datasetuspto-grants-2015_01
ORD IDord-ab4998f89b47400a8c8b424fbe711bca
Source noteuspto-grants-2015_01