Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382937Generated: October 30, 2026

Pyrazine, 2-(chloromethyl)- → HCID 18361795, compound

https://huagongshe.com/reaction/382937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazine, 2-(chloromethyl)-HCID 170169—
ReactantHCID 18361721HCID 18361721—
ReactantHCID 178435601HCID 178435601—
ProductHCID 18361795HCID 18361795—

Reaction Steps

The title-compound was prepared from 6-hydroxy-3-(5-ethylisoxazol-3-yl)-1,2,4-triazolo[3,4-a]phthalazine (prepared from 6-chloro-3-(5-ethylisoxazol-3-yl)-1,2,4-triazolo[3,4-a]phthalazine, Example 105 part c, using conditions described for the preparation of Intermediate 2) and 2-chloromethylpyrazine (prepared as described in Example 15 part a) using the procedure described in Example 15 part b, 1H NMR (360 MHz, CDCl3) δ 1.42 (3H, t, J=7.6 Hz, CH3), 2.94 (2H, q, J=7.6 Hz, CH2), 5.83 (2H, s, CH2), 6.84 (1H, s, Ar—H), 7.84 (1H, m, Ar—H), 7.98 (1H, m, Ar—H), 8.30 (1H, d, J=7.9 Hz, Ar—H), 8.60-8.64 (2H, m, 2 of Ar—H), 8.70 (1H, m, Ar—H), 9.15 (1H, d, J=1.3 Hz, Ar—H); MS (ES+) m/e 374 [MH]+; Anal. Found. C, 61.16; H, 3.79; N, 26.19. C19H15N7O2 requires C, 61.12; H, 4.05; N, 26.26%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310203B1
Source datasetuspto-grants-2001_10
ORD IDord-18a7cc7cd4004a5881bc5e8bc9b96773
Source noteuspto-grants-2001_10