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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934888Generated: November 3, 2026

Water → HCID 18739877, compound

https://huagongshe.com/reaction/1934888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 18739873HCID 18739873—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18739877HCID 1873987766.7%

Reaction Steps

To a stirred solution of (1S,2R,3S,4R)-3-(1-benzothien-5-yl)-N,N-dimethylbicyclo[2,2,1]heptane-2-carboxamide (200 mg, 0.67 mmol) in dry tetrahydrofuran (5 mL) at −78° C. was added lithium diisopropylamide (1.67 mL, 3.35 mmol). The mixture was stirred at this temperature for 1 hour before iodomethane (2.3 mL, 3.35 mmol) was added. The mixture was stirred for another 10 minutes at this temperature before it was allowed to warm to room temperature. After 1 hour, water was added and the layers were separated. The aqueous phase was extracted with ethyl acetate (2×10 mL) and the extracts were washed with water (2×10 mL) dried over magnesium sulphate and evaporated in-vacuo. Column chromatography with 20% ethyl acetate in hexane provided the (1S,2R,3S,4R)-3-(2-methyl-1-benzothien-5-yl)-N,N-dimethylbicyclo [2,2,1]heptane-2-carboxamide as a glass (140 mg, 66%). M/e 314 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384281B1
Source datasetuspto-grants-2002_05
ORD IDord-6f14cc5a0dd7445a868a4ef3f0f88bc1
Source noteuspto-grants-2002_05