Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641159Generated: October 31, 2026

Thionyl Chloride → HCID 12109145, compound

https://huagongshe.com/reaction/641159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 12109144HCID 12109144—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 12109145HCID 12109145—

Reaction Steps

To a solution of (R)-4-(1-benzyloxycarbonylaminoethyl)-benzoic acid (1.2 g) in dichloromethane (15 mL) were added thionyl chloride (0.9 mL) and one drop of dimethylformamide, and the mixture was stirred at room temperature for 2 hrs. After the reaction, the solvent was evaporated under reduced pressure to give (R)-4-(1-benzyloxycarbonylaminoethyl)benzoic acid chloride as crystals. Then, the crystals were dissolved in acetonitrile (10 mL) and added dropwise to a solution of 4-amino-1H-pyrrolo[2,3-b]pyridine (240 mg) and diisopropylethylamine (520 mg) in acetonitrile (10 mL), and the mixture was stirred at room-temperature for 8 hrs. The precipitated crystals were collected by filtration, dried and dissolved in methanol (7 mL). Sodium methoxide (60 mg) was added and the mixture was stirred at room temperature for 30 min. After the reaction, the mixture was concentrated under reduced pressure. Water was added to the obtained residue and the mixture was extracted with ethyl acetate. The extract was dried and the solvent was evaporated under reduced pressure. The obtained crystals were washed with ethyl acetate to give (R)—N-(1H-pyrrolo[2,3-b]pyridin-4-yl)-4-(1-benzyloxycarbonylaminoethyl)benzamide (330 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696194B2
Source datasetuspto-grants-2010_04
ORD IDord-5ad9a375c99e4c3da730bcb4d932cf21
Source noteuspto-grants-2010_04