반응 #332688

ord-c6dcf7c953e5453cb9a0719b9b717f07

반응 방정식

[BH4-].[Na+]
NaBH4
FB(F)F
BF3
B#B
diborane
Cc1noc2c(Cl)c(N3C[C@@H](C)O[C@@H](C)C3)c(C(=O)O)cc12
7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazole-5-carboxylic acid
Cc1noc2c(Cl)c(N3C[C@@H](C)O[C@@H](C)C3)c(C(=O)O)cc12
Intermediate 302
Cc1noc2c(Cl)c(N3C[C@@H](C)O[C@@H](C)C3)c(C(=O)O)cc12
7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazole-5-carboxylic acid
Cc1noc2c(Cl)c(N3C[C@@H](C)O[C@@H](C)C3)c(CO)cc12
{7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazol-5-yl}methanol

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타before being quenched with methanol (1 mL)
  2. 2
    농축concentrated
  3. 3
    기타The residue was purified by column chromatography
  4. 4
    기타to give product as solid

실험 절차

To a stirred solution of NaBH4 (78 mg, 2.43 mmol) in diglyme (1 mL) was added BF3 (1.6 mL, 2.59 mmol), and the thus generated diborane gas was purged into solution of 7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazole-5-carboxylic acid (Intermediate 302, 250 mg, 0.8 mmol) in THF (1 mL). The mixture was stirred at room temperature for 30 minutes before being quenched with methanol (1 mL) and concentrated. The residue was purified by column chromatography to give product as solid. Yield: 130 mg (52%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08658641B2uspto-grants-2014_02