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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748274Generated: October 30, 2026

Hydrochloric Acid → HCID 67235300, compound

https://huagongshe.com/reaction/1748274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl 1H-indole-2,6-dicarboxylateHCID 44754779—
ReactantHCID 86682389HCID 86682389—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67235300HCID 6723530069.4%

Reaction Steps

A stirred suspension of 60% NaH (840 mg, 21 mmol) in NMP (40 mL) is cooled in an ice bath, and a solution of diethyl 1H-indole-2,6-dicarboxylate (Intermediate A, 5.8 g, 22 mmol) in NMP (20 mL) is added. The mixture is stirred for 20 min, then a solution of tert-butyl (6S)-6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxide (5.0 g, 20 mmol) in NMP (20 mL) is added. The reaction mixture is stirred for 30 min at 0° C. and is warmed to room temperature and stirred for 48 h. The reaction is poured into ice water and the resultant solid is isolated by filtration. The filtrate is acidified to pH 3 with 1N aqueous HCl and extracted with EtOAc. The combined extracts are washed with water 4 times, then brine, dried (Na2SO4) and concentrated to afford the title compound (6.0 g, crude) as an oil which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-d27cfdc986a44fd3834d54c992acd55f
Source noteuspto-grants-2015_10