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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094896Generated: November 1, 2026

HCID 57955155, compound → HCID 57955292, compound

https://huagongshe.com/reaction/1094896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57955155HCID 57955155—
ReactantHCID 57955235HCID 57955235—
ProductHCID 57955292HCID 5795529223%

Reaction Steps

The title compound was prepared in a manner similar to the procedure described for the preparation of Example 87, using N-{4-[4-amino-6-(hydroxymethyl)-7-(morpholin-4-ylmethyl)pyrrolo[2,1-f]-[1,2,4]triazin-5-yl]-2-fluorophenyl}-N′-[4-(trifluoro-methyl)-pyridin-2-yl]urea (which can be prepared using the procedure used for the preparation of Example 62 substituting Intermediate AJ for Intermediate Y) in place of Example 85 (N-{4-[4-amino-6-formyl-7-(morpholin-4-ylmethyl)pyrrolo[2,1-f]-[1,2,4]triazin-5-yl]phenyl}-N′-[4-(trifluoro-methyl)pyridin-2-yl]urea), 45 mg (23%) of the desired product was isolated. 1H-NMR (DMSO-d6) δ 10.16-10.10 (m, 2H), 8.54 (d, J=5.1 Hz, 1H), 8.31 (t, J=8.4 Hz, 1H), 8.01 (s, 1H), 7.95 (s, 1H), 7.39-7.19 (m, 3H), 5.35 (d, J=49.8 Hz, 2H), 3.92 (s, 2H), 3.53-3.52 (m, 4H), 2.48-2.43 (m, 4H); MS [M+H]+=562.7; LCMS RT=2.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133995B2
Source datasetuspto-grants-2012_03
ORD IDord-d2db66a4c9774cff9c393bddb5252970
Source noteuspto-grants-2012_03