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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187075Generated: November 1, 2026

Methanesulfonyl chloride → HCID 22449872, compound

https://huagongshe.com/reaction/2187075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22449735HCID 22449735—
ProductHCID 22449872HCID 2244987258%

Reaction Steps

Using the method similar to that in Example 43 and methanesulfonyl chloride (190 ml, 2.45 mmol) instead of ethylmalonyl chloride and starting from 6-amino-2,4-dioxo-1-[4-(4-diphenylmethoxypiperidino)butyl]-1,2,3,4-tetrahydroquinazoline (1.02 g, 2.05 mmol) obtained in Example 40, a free salt of the title compound (681 mg, 58%) was synthesized. Recrystallization from ethyl acetate yielded a colorless crystal having a melting point of 204 to 205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407116B1
Source datasetuspto-grants-2002_06
ORD IDord-07499cd819ef48e4a3356f5972b0b82a
Source noteuspto-grants-2002_06