Allyl chloroformate → HCID 16045476, compound

HRID 2354922Notes

Reaction equation

[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:19]3[CH2:20][CH2:21][CH2:22][CH:12]2[C:13]2[CH:14]=[N:15][NH:16][C:17]=2[CH2:18]3)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH2:23]([O:26][C:27](Cl)=[O:28])[CH:24]=[CH2:25]>>[CH2:23]([O:26][C:27]([N:15]1[N:16]=[C:17]2[C:13]([CH:12]3[N:11]([S:8]([C:5]4[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=4)(=[O:9])=[O:10])[CH:19]([CH2:18]2)[CH2:20][CH2:21][CH2:22]3)=[CH:14]1)=[O:28])[CH:24]=[CH2:25]

Participants

Reactant 2

HCID 18052Allyl chloroformate

HCID 16045311HCID 16045311, compound

Product 1

HCID 16045476HCID 16045476, compound

Procedure

Prepared by acylation of 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-diene using allylchloroformate

Sources & evidence

ORD record: ord-7322f41bf80a4eb79383410e05b5f589
Source dataset: uspto-grants-2010_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07754712B2

Reaction notes

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