반응 #77165

ord-cab98f97cc574977b1563c92ed4183bb

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타as prepared in step 3 of Example 1

실험 절차

The title compound was prepared from 3-chlorobenzylsulfonyl chloride (113 mg, 0.5 mmol), as prepared in the preceding step, and 3-amino-6-methyl-1-(tert-butoxycarbonylmethyl)-2-pyridinone (120 mg, 0.5 mmol), as prepared in step 3 of Example 1, using the procedure in step 4 of Example 1, as a white solid (180 mg, 84%). 1H-NMR (300 MHz, CDCl3) δ7.37 (d, J=7.6 Hz, 1H), 7.30 (m, 4H), 7.20 (s, 1H), 6.02 (d, J=7.7 Hz, 1H), 4.78 (s, 2H), 4.27 (s, 2H), 2.27 (s, 3H), 1.50 (s, 9H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06706021B2uspto-grants-2004_03