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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072549Generated: October 30, 2026

Methane → 300843-20-3

https://huagongshe.com/reaction/1072549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantMethanolHCID 887—
ReactantVatalanibHCID 151194—
Product300843-20-3HCID 22386458—

Reaction Steps

Heating of a mixture of 1-(4-chloranilino)-4-(4-pyridylmethyl)-phthalazine (Example 4 in WO 98/35958) and charcoal in boiling methanol for about 7 days in an open vessel leads to partial oxidation of the methylen-bridge of 1-(4-chloranilino)-4-(4-pyridylmethyl)-phthalazin. After cooling to RT, unchanged 1-(4-chloranilino)-4-(4-pyridylmethyl)-phthalazine crystallizes out and can be filtered off. Chromatography (SiO2; dichloromethane/methanol 98:2) of the concentrated filtrate then leads to [4-(4-chloranilino)phthalazin-1-yl](pyridin-4-yl)ketone and rac. [4-(4-chloranilino)phthalazin-1-yl](pyridin-4-yl)methanol (see Expl. 78 in WO 98/35958). [4-(4-Chloranilino)phthalazin-1-yl](pyridin-4-yl)ketone: 1H NMR (DMSO-d6) δ 9.88 (bs, 1H, HN), 8.79 (d, 2H, pyridine), 8.71 (d, 1H), 8.63 (d, 1H), 8.07 (m, 2H), 7.97 (d, 2H, chloranilino), 7.77 (d, 2H, pyridine), 7.45 (d, 2H, chloranilino); IR (KBr): 3287, 3139, 3066, 1667 (CO), 1620 cm−1; FAB MS (M+H)+=361.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911440B2
Source datasetuspto-grants-2005_06
ORD IDord-3994a428c6ac45c1846a29bca3d58a39
Source noteuspto-grants-2005_06