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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10263Generated: October 28, 2026

Ammonium Chloride → HCID 178418829, compound

https://huagongshe.com/reaction/10263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantBenzylsulfamic acid [6-chloro-2-(2-cyano-pyridin-4-yl)-5-(2-methoxy-phenoxy) pyrimidin-4-yl]-amideHCID 21041243—
SolventDimethylformamideHCID 6228—
ProductHCID 178418829HCID 17841882937%

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzylsulfamic acid [6-chloro-2-(2-cyano-pyridin-4-yl)-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide (4.17 g) was dissolved in DMF (55 ml). Sodium azide (5.2 g) and ammonium chloride (4.28 g) were added and the mixture was stirred for 20 h at 80° C. Then the mixture was pored onto water and extracted with EtOAc. The layers were separated and the water layer was acidified with acetic acid to pH ˜5 and extracted with EtOAc. The combined organic layers from the 2nd extraction were washed with brine, dried over magnesium sulfate, filtered and evaporated. The crude material was purified by chromatography over silicagel with EtOAc/MeOH/ammonia=5/1/0.5 to give benzylsulfamic acid [6-chloro-5-(2-methoxy-phenoxy)-2-[2-(1H-tetrazol-5-yl)-pyridin-4-yl]-pyrimidin-4-yl]-amide (1.67 g). LC-MS: tR=5.02; [M+H]+=566.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094781B2
Source datasetuspto-grants-2006_08
ORD IDord-0b976c54799a443abc1b8ade62e50a2f
Source noteuspto-grants-2006_08