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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165585Generated: October 28, 2026

Triethylamine → HCID 14676879, compound

https://huagongshe.com/reaction/1165585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantHCID 14676869HCID 14676869—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14676879HCID 1467687987%

Reaction Steps

A solution of 4-methylaminomethyl-5-methyl-2,3,4,5-tetrahydrothiopyrano[3,2-b]indole (3.2 g) in dry tetrahydrofuran (30 ml) is allowed to react with triethylamine and 2-t-butoxycarbonyloxyimino-2-phenylacetonitrile in the same manner as in Example 6(a) to give 4-(N-methyl-N-t-butoxycarbonylaminomethyl)-5-methyl-2,3,4,5-tetrahydrothiopyrano[3,2-b]indole: Yield 87.0%. Mp. 111.5°-114° C. (decomp.) (b) The above product is treated in the same procedure as in Example 12 to give 4-(N-methyl-N-t-butoxycarbonylaminomethyl)-5-methyl-2,3,4,5-tetrahydrothiopyrano[3,2-b]indole 1-oxide. Mp. 218°-220.5° C. (decomp.). The product is dissolved in methylene chloride (20 ml) and trifluoroacetic acid (4 ml) is added thereto. The mixture is kept at room temperature for 2 hours and then treated in the usual manner to give the title compound (1.13 g): Yield 89.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910318
Source datasetuspto-grants-1990_03
ORD IDord-089862cf29734febaa6c023c925774fe
Source noteuspto-grants-1990_03