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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903922Generated: October 30, 2026

Tert-Butylamine → HCID 23335502, compound

https://huagongshe.com/reaction/903922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantHCID 23335530HCID 23335530—
ProductHCID 23335502HCID 2333550255%

Reaction Steps

1.5 g of 4-(2,3-epoxypropoxy)-2-carbamoyl-6-methyl indole in 25 ml tert.-butylamine is heated to boiling for 24 hours. The solution is then evaporated and the residue dissolved in chloroform. The chloroform solution is washed with water, dried and evaporated. The residue is suspended in hot acetic ester and mixed with 0.8 g benzoic acid. A clear solution will result here, from which a precipitate deposits. This is aspirated and recrystallized from 100 ml acetic ester. There is obtained 1.5 g (55% of theory) 4-(2-hydroxy-3-tert.-butylaminopropoxy)-2-carbamoyl-6-methyl indole as benzoate; m.p. 213°-214° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229464
Source datasetuspto-grants-1980_10
ORD IDord-d5b4616308f64dc4a93e5e2d5e6b4f82
Source noteuspto-grants-1980_10