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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817703Generated: November 1, 2026

Formaldehyde → HCID 16062917, compound

https://huagongshe.com/reaction/1817703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHCID 66616339HCID 66616339—
SolventFormic AcidHCID 284—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 16062917HCID 16062917—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-(4-fluoro-benzyl)-4-(4-fluoro-phenyl)-5,6,8,9-tetrahydro-pyrimido[4,5-d]azepine-7-carboxylic acid tert-butyl ester in formic acid was added paraformaldehyde (10 equiv.). The mixture was heated at 80° C. for 6 h. The mixture was diluted with water and basified to pH ˜10 with 1 M NaOH. The mixture was extracted with CH2Cl2, dried and concentrated. Chromatography on SiO2 (0-5% 2 M NH3 in MeOH/CH2Cl2) afforded the desired compound. 2-(4-Fluoro-benzyl)-4-(4-fluoro-phenyl)-7-methyl-6,7,8,9-tetrahydro-5H-pyrimido[4,5-d]azepine was also obtained. MS (ESI): exact mass calcd. for C23H21F2N3, 377.17; m/z found, 378.4 [M+H]+. 1H NMR (CDCl3): 7.50-7.46 (m, 2H), 7.42-7.37 (m, 2H), 7.17-7.12 (m, 2H), 6.99-6.94 (m, 4H), 6.03-6.01 (m, 1H), 5.47-5.46 (m, 1H), 4.25 (s, 2H), 3.51 (s, 2H), 2.87-2.83 (m, 2H), 2.76-2.72 (m, 2H), 2.41 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598255B2
Source datasetuspto-grants-2009_10
ORD IDord-df9391a187344856a59898c6fa6c4ca2
Source noteuspto-grants-2009_10