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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626829Generated: November 2, 2026

Dichloromethane → HCID 71765551, compound

https://huagongshe.com/reaction/626829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86697522HCID 86697522—
ProductHCID 71765551HCID 71765551—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl (3S)-9-[1-(4-amino-3-methyl-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl]-7-chloro-6-fluoro-3-methyl-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (13 mg, 0.026 mmol) was stirred in methylene chloride (100 μL, 2 mmol) with N,N-diisopropylethylamine (14 μL, 0.079 mmol) and cooled to 0° C. Methanesulfonyl chloride (2.6 μL, 0.034 mmol) was added, and the mixture was stirred at 0° C. for 1 hr. The mixture was evaporated and diluted with methanol. The reactions were purified by prep HPLC on C-18 column eluting water:acetonitrile gradient buffered pH 10 to give two enantiomers: Peak #1 (Example 35): LCMS calculated for C19H23ClFN6O3S (M+H)+: m/z=469.1; found: 469.1; Peak #2 (Example 36): LCMS calculated for C19H23ClFN6O3S (M+H)+: m/z=469.1; found: 469.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309251B2
Source datasetuspto-grants-2016_04
ORD IDord-f9381b06773a40bcaf13f2a69e3e59d8
Source noteuspto-grants-2016_04