Sodium hydride → HCID 53241085, compound

HRID 1475986Notes

Reaction equation

HRID 1475986 reaction equation
[C:1]([O:4][NH:5][C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])(=[O:3])[CH3:2].[H-].[Na+].[O:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH:17]=[C:16]1[S:24](Cl)(=[O:26])=[O:25]>>[C:1]([O:4][N:5]([C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])[S:24]([C:16]1[O:15][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[CH:17]=1)(=[O:25])=[O:26])(=[O:3])[CH3:2]

Participants

4

Reactant 3

HCID 24758Sodium hydrideHCID 27951721-Benzofuran-2-sulfonyl chlorideHCID 10058028(ACETYLOXY)-CARBAMIC ACID TERT-BUTYL ESTER

Product 1

HCID 53241085HCID 53241085, compound

Procedure

N-[(tert-Butoxy)carbonyl]1-benzofuran-2-sulfonamido acetate (105) is prepared from [(tert-butoxy)carbonyl]amino acetate, sodium hydride and 1-benzofuran-2-sulfonyl chloride according to Scheme 2. δH (250 MHz, DMF) 8.07 (1H, d, 0.9 Hz), 7.91 (1H, d, 7.3 Hz), 7.82 (1H, dd, 8.5, 0.8 Hz), 7.64 (1H, td, 7.8, 1.4 Hz), 7.41-7.52 (1H, m), 2.32 (3H, s), 1.37 (9H, s).

Sources & evidence

ORD record
ord-6e92901855814e598c2ee74dc94ed084
Source dataset
uspto-grants-2015_04
Patent number
US09018411B2

Reaction notes

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