反应 #2487499

ord-4494aa9e81334d518bd1f9c27e0d0b96

反应方程式

CC(C)(C)OC(=O)[C@@H](N)CCC(=O)O
H-Glu-OtBu
CCN(C(C)C)C(C)C
DIPEA
CC(C)(C)OC(=O)c1ccc(CCCCCCCCCCCCC(=O)O)s1
5-(12-carboxydodecyl)-thiophene-2-carboxylic acid tert-butyl ester
CN(C)C(ON1C(=O)CCC1=O)=[N+](C)C.F[B-](F)(F)F
TSTU
CCN(C(C)C)C(C)C
DIPEA
CC(C)(C)OC(=O)c1ccc(CCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)O)C(=O)OC(C)(C)C)s1
(S)-2-[13-(5-tert-Butoxycarbonylthiophen-2-yl)-tridecanoylamino]-pentanedioic acid 1-tert-butyl ester

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solvent was removed in vacuo
  2. 2
    其他The mixture was separated between diethyl ether (10 mL) and 10% aqueous NaHSO4 (2×10 mL)
  3. 3
    其他the organic phase isolated
  4. 4
    其他solvent removed in vacuo

实验过程

5-(12-carboxydodecyl)-thiophene-2-carboxylic acid tert-butyl ester (31 mg, 0.0 78 mmol) was treated with TSTU (28.2 mg, 0.094 mmol) and DIPEA (0.016 mL, 0.094 mmol) in THF (1.3 mL) for 2½ hours at room temperature under nitrogen. The solvent was removed in vacuo and the mixture added NMP (1 mL) and H-Glu-OtBu (31.3 mg, 0.154 mmol) and DIPEA (0.027 mL). The mixture was stirred overnight at room temperature. The mixture was separated between diethyl ether (10 mL) and 10% aqueous NaHSO4 (2×10 mL) and the organic phase isolated and solvent removed in vacuo to give the crude (S)-2-[13-(5-tert-Butoxycarbonylthiophen-2-yl)-tridecanoylamino]-pentanedioic acid 1-tert-butyl ester which was subsequently in the next step without any further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08796205B2uspto-grants-2014_08