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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045870Generated: October 30, 2026

5-(Trifluoromethyl)pyrazine-2-carboxylic acid → N-(3-((4aS,5S,7aS)-2-amino-5-(trifluoromethyl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-7a-yl)-4-fluorophenyl)-5-(trifluoromethyl)pyrazine-2-carboxamide

https://huagongshe.com/reaction/2045870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Trifluoromethyl)pyrazine-2-carboxylic acidHCID 55262854—
Reactanttert-butyl[(4aS,5S,7aS)-7a-(5-amino-2-fluorophenyl)-5-trifluoromethyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]carbamateHCID 68171522—
ProductN-(3-((4aS,5S,7aS)-2-amino-5-(trifluoromethyl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-7a-yl)-4-fluorophenyl)-5-(trifluoromethyl)pyrazine-2-carboxamideHCID 57523782—

Reaction Steps

Synthesized from tert-butyl [(4aS,5S,7aS)-7a-(5-amino-2-fluorophenyl)-5-trifluoromethyl-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]carbamate and 5-trifluoromethylpyrazine-2-carboxylic acid according to the general procedure. 1H NMR (400 MHz, CDCl3) δ ppm 2.80 (dd, J=13.6, 3.8 Hz, 1H), 3.11 (dd, J=13.8, 2.9 Hz, 1H), 3.30-3.44 (m, 1H), 3.87 (d, J=8.3 Hz, 1H), 4.25-5.14 (m, 4H), 7.07 (dd, J=11.9, 8.8 Hz, 1H), 7.57 (dd, J=6.8, 2.8 Hz, 1H), 7.86 (dt, J=8.4, 3.6 Hz, 1H), 8.89 (s, 1H), 9.53 (s, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592408B2
Source datasetuspto-grants-2013_11
ORD IDord-b7ef2fdab62a4f8ab3982a0d9a3934b0
Source noteuspto-grants-2013_11