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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600470Generated: October 30, 2026

Oxalyl chloride → HCID 59729271, compound

https://huagongshe.com/reaction/600470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59729278HCID 59729278—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59729271HCID 597292711,042.6%

Reaction Steps

Oxalyl chloride (4.5 mL, 51 mmol) was added to a solution of diazaindole carboxylic acid 50 (1.08 g, 4.7 mmol) in CH2Cl2 (8 mL) and the reaction mixture was stirred 14 h. Catalytic DMF (3 drops) was added to the reaction mixture and after 3 h the reaction was quenched with MeOH. The crude reaction mixture was concentrated to dryness to yield 51 (1.21 g, 49 mmol, 96%) as a tan solid with was used without further purification. 1H NMR: (500 MHz, DMSO-d6) δ 12.45 (br s, 1H), 8.87 (s, 1H), 8.87 (d, J=2.6 Hz, 1H), 8.32 (d, J=3.3 Hz, 1H), 8.14 (d, J=1.5 Hz, 1H), 6.77 (dd, J=2.6, 1.5 Hz, 1H); Methyl ester (obtained by stirring 51 in MeOH): LC/MS: (ES+) m/z (M+H)+=244; HPLC Rt=0.95 min., column 0, conditions B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902204B2
Source datasetuspto-grants-2011_03
ORD IDord-be9eda7b0b2f40349804e0bb41c6db86
Source noteuspto-grants-2011_03