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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003924Generated: October 26, 2026

Pyridine → Ammonia dichloromethane

https://huagongshe.com/reaction/1003924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418337HCID 178418337—
ReactantHCID 178484888HCID 178484888—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductAmmonia dichloromethaneHCID 22731429—
ProductHCID 178418337HCID 178418337—

Reaction Steps

TBDMS protected histidinol 14--To a stirred solution of 205 mg (5.1 mmol) of NaH washed 3× with hexane, under argon, in 3.0 mL DMF was added in portions 500 mg (2.3 mmol) of N-methylhistidinol dihydrochloride, resulting in moderate gas evolution. The solution was stirred for 1.5 h, then 1.8 mL (23 mmol) of anhydrous pyridine and 693.0 mg (4.6 mmol) of TBDMSC1 was added. The solution was stirred for 1.5 h, concentrated in vacuo and flash chromatographed on silica with 15% CH3OH.NH3 /CH2Cl2 to yield 14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048698
Source datasetuspto-grants-2000_04
ORD IDord-263e2b32bca64b08bf275a1181b01497
Source noteuspto-grants-2000_04