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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433065Generated: November 1, 2026

Dimethylformamide → HCID 86592558, compound

https://huagongshe.com/reaction/1433065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 9948722HCID 9948722—
ReactantHCID 12330501HCID 12330501—
ProductHCID 86592558HCID 86592558—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-chloro-thiophene-2-carbonyl azide (28 mg, 0.15 mmol, EXAMPLE 38) and 4-[4-Amino-quinazolin-7-ylmethyl]-5-methyl-3-oxo-2-propyl-piperazine, EXAMPLE 888, (26 mg, 0.08 mmol) in 3 mL of dry DMF is heated at 100° C. for 1 h. The resulting mixture is concentrated in vacuo. The crude product is purified by RP-HPLC eluting in a gradient of 10% CH3CN/H2O (0.1% TFA) to 70% CH3CN/H2O (0.1% TFA) and the appropriate product fractions are combined and lyophilized to provide the title compound (18 mg, 0.03 mmol) as a white solid. 1H NMR (d6-DMSO, 300 MHz) δ9.96 (bs, 1H), 9.70 (bs, 2H), 8.72 (s, 1H), 8.22 (d, 1H), 7.55 (d, 1H), 7.50 (s, 1H), 6.68 (d, 1H), 6.37 (d, 1H), 4.99-4.38 (m, 3H, rotamers), 4.15 (m, 1H, rotamers), 3.58 (m, 1H, rotamers), 3.10 (m, 1H), 1.85 (m, 2H), 1.32 (m, 2H), 1.07 (m, 3H, rotamers), 0.88 (t, 3H). ISP MS, [M+H]+=473, 475 (Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-465773de76c944b09e5677808b448aed
Source noteuspto-grants-2009_11