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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284892Generated: October 31, 2026

Allyl bromide → HCID 13321945, compound

https://huagongshe.com/reaction/1284892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 13321944HCID 13321944—
ReactantDiazabicycloundecaneHCID 57346892—
SolventEthanolHCID 702—
ProductHCID 13321945HCID 13321945—

Reaction Steps

Under argon, 0.4 g of 8-amino-5H-pyrimido[5,4-b]indole-2-carboxylic acid ethyl ester (Example 11) is agitated in 8 ml of ethanol with 0.16 ml of diazabicycloundecane and 0.25 ml of allyl bromide for 5 hours at 50°-60° C. The reaction solution is subsequently evaporated, and the residue is taken up in ethyl acetate. This solution is washed first with water, then with sodium bicarbonate solution, and finally again with water, dried with sodium sulfate, and concentrated, thus obtaining 0.18 g of 8-diallylamino-5H-pyrimido[5,4-b]indole-2-carboxylic acid ethyl ester, mp 188°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564610
Source datasetuspto-grants-1986_01
ORD IDord-60413556497d47c5b3c0e324d2b6d36d
Source noteuspto-grants-1986_01