HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 13321945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 13321944 | HCID 13321944 | — |
| Reactant | Diazabicycloundecane | HCID 57346892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13321945 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04564610 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-60413556497d47c5b3c0e324d2b6d36d |
| Source note | uspto-grants-1986_01 |