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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902166Generated: October 29, 2026

Triethylamine → 1'-(1,1-Dimethylethyloxycarbonyl)-3-(methylsulfonyl)amino-2,3-dihydrospiro(1H-indene-1,4'-piperidine)

https://huagongshe.com/reaction/1902166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 3-amino-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylateHCID 18476131—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1'-(1,1-Dimethylethyloxycarbonyl)-3-(methylsulfonyl)amino-2,3-dihydrospiro(1H-indene-1,4'-piperidine)HCID 23367999—

Reaction Steps

A sample of 1'-(1,1-Dimethylethyloxycarbonyl)-3-amino-2,3-dihydrospiro(1H-indene-1,4'-piperidine), prepared by hydrogenation of 500 mg of oxime (1.58 mmole) as in Example 135 Step A, in 3.5 mL methylene chloride containing 475 mg of DMAP (2.46×1.58 mmole), and 550λ of triethylamine (2.51×1.58 mmole), was stirred under nitrogen in an ice bath while adding a solution of 270λ of methanesulfonyl chloride (2.2×1.58 mmole) in 3 mL methylene chloride dropwise over 2-3 minutes. The suspension was stored over night in the refrigerator. It was then washed twice with water, dried with magnesium sulfate and concentrated under reduced pressure to a gum. Preparative TLC on four 8"×8"×1,000 g GF silica gel plates using 1:2 ethyl acetate: hexane afforded the title compound, which crystallized on standing. Yield: 322 mg (54%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578593
Source datasetuspto-grants-1996_11
ORD IDord-393c9f8390c94906a37c4d7b3eb3dab2
Source noteuspto-grants-1996_11