Ethyl Bromide → HCID 10798542, compound

HRID 2210459Notes

Reaction equation

HRID 2210459 reaction equation
[S:1]1(=[O:12])(=[O:11])[C:6]2[N:7]=[CH:8][CH:9]=[CH:10][C:5]=2[NH:4][CH:3]=[N:2]1.[CH2:13](Br)[CH3:14]>>[CH2:13]([N:4]1[C:5]2[CH:10]=[CH:9][CH:8]=[N:7][C:6]=2[S:1](=[O:12])(=[O:11])[N:2]=[CH:3]1)[CH3:14]

Participants

3

Reactant 2

HCID 6332Ethyl BromideHCID 9989901HCID 9989901, compound

Product 1

HCID 10798542HCID 10798542, compound

Procedure

The compound is obtained according to the same procedure as that described for Example 63, starting from 0. 1 g of 4H-pyrido[3,2-e][1,2,4]thiadiazine 1,1-dioxide (Example 16) and 0.17 g of ethyl bromide.

Workup

  1. customThe compound is obtained

Sources & evidence

ORD record
ord-b9c394c0d8054d09b2d0c8a29f54b6b7
Source dataset
uspto-grants-1995_10
Patent number
US05459138

Reaction notes

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