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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514067Generated: October 30, 2026

2-Bromopyrimidine → HCID 56599529, compound

https://huagongshe.com/reaction/514067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyrimidineHCID 78345—
ReactantHCID 67126276HCID 67126276—
ProductHCID 56599529HCID 56599529—

Reaction Steps

(S)-2-tert-butoxy-2-(1-(4-chlorophenyl)-3-methyl-6-(pyrazin-2-yl)naphthalen-2-yl)acetic acid was prepared in a similar fashion to compound 59 with the substitution of 2-chloropyrazine for 2-bromopyrimidine in step 2. The title compound (0.026 g) was isolated as an amorphous pale yellow powder. LCMS-ESI+ (m/z): [M+H]+ calcd for C27H26ClN2O3: 461.96; found: 461.30. 1H-NMR: 400 MHz, (CD3CN) δ: 9.23 (s, 1H); 8.67 (s, 1H); 8.56 (s, 2H); 8.05 (d, J=8.8 Hz, 1H); 7.89 (s, 1H); 7.61-7.54 (m, 3H); 7.42 (d, J=8.8 Hz, 1H); 7.39 (br d, J=8.8 Hz, 1H); 5.23 (s, 1H); 2.60 (s, 3H); 1.00 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102614B2
Source datasetuspto-grants-2015_08
ORD IDord-a50e6fae70c14cefba5db8302b0ed675
Source noteuspto-grants-2015_08